Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

R AND D BATTERIES, INC. PART NOS. 5038 & 5347

K-Number: K933491 · 1993-11-19

ApplicantR & D Batteries, Inc.
Decision Date1993-11-19
Product CodeETN
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

R AND D BATTERIES, INC. PART NOS. 5038 & 5347 is the device name listed in this FDA 510(k) record. The listed applicant is R & D Batteries, Inc.. It received FDA 510(k) clearance on 1993-11-19 under 510(k) number K933491. The device is classified under product code ETN. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the R AND D BATTERIES, INC. PART NOS. 5038 & 5347?

R AND D BATTERIES, INC. PART NOS. 5038 & 5347 is a medical device that received FDA 510(k) clearance on 1993-11-19. The listed applicant is R & D Batteries, Inc.. The 510(k) number is K933491.

When did R AND D BATTERIES, INC. PART NOS. 5038 & 5347 receive FDA 510(k) clearance?

R AND D BATTERIES, INC. PART NOS. 5038 & 5347 received FDA 510(k) clearance on 1993-11-19, under 510(k) number K933491.

Who is the listed applicant for R AND D BATTERIES, INC. PART NOS. 5038 & 5347?

The FDA 510(k) record lists R & D Batteries, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for R AND D BATTERIES, INC. PART NOS. 5038 & 5347?

The FDA product code for R AND D BATTERIES, INC. PART NOS. 5038 & 5347 is ETN.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing R & D Batteries, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K951284R&D BATTERIES, INC. PART NUMBERS 5137, 5140, 5142 AND 5155K951277R&D BATTERIES, INC. PART NUMBERS 5295, 5334, 5344 AND 5410K951278R&D BATTERIES, INC. PART NUMBERS 5213, 5222, 5268 AND 5284K951280R&D BATTERIES, INC. PART NUMBERS 5003, 5006, 5008 AND 5012K951285R&D BATTERIES, INC. PART NUMBERS 5158, 5168, 5171 AND 5172K951276R&D BATTERIES, INC. PART NUMBERS 5412, 5420, 5436 AND 5438

View all 52 devices →

Related Devices (Code: ETN)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K253536Evala Nerve Stimulator (EPNR002)Epineuron Technologies, Inc.K251672NIM Essence™ EMG Endotracheal Tube (NIMEID060); NIM Essence™ EMG Endotracheal Tube (NIMEID065); NIM Essence™ EMG Endotracheal Tube (NIMEID070); NIM Essence™ EMG Endotracheal Tube (NIMEID075); NIM Essence™ EMG Endotracheal Tube (NIMEID080)Medtronic Xomed, Inc.K242852ALM Tube I.D. 6.0, O.D. 8.2 (520843), ALM Tube I.D. 7.0, O.D. 9.7 (520845), ALM Tube I.D. 7.5, O.D. 10.3 (520846), ALM Tube I.D. 8.0, O.D. 11.0 (520847)Inomed Medizintechnik GmbHK233001Bioscope Neuromonitor DeviceBiosys Biyomedikal Muhendislik San. VE Tic. A.S.K241917EARP Nerve Cuff ElectrodeRetropsoas Technologies, LLCK232888Disposable Laryngeal ElectrodesSuzhou Haishen Medical Device Associates Co., Ltd.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

↑