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FDA 510(k)

RECHARGEABLE BATTERIES

K-Number: K944521 · 1995-03-06

ApplicantR & D Batteries, Inc.
Decision Date1995-03-06
Product CodeFCO
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

RECHARGEABLE BATTERIES 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 1995-03-06 under 510(k) number K944521. The device is classified under product code FCO. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RECHARGEABLE BATTERIES?

RECHARGEABLE BATTERIES is a medical device that received FDA 510(k) clearance on 1995-03-06. The listed applicant is R & D Batteries, Inc.. The 510(k) number is K944521.

When did RECHARGEABLE BATTERIES receive FDA 510(k) clearance?

RECHARGEABLE BATTERIES received FDA 510(k) clearance on 1995-03-06, under 510(k) number K944521.

Who is the listed applicant for RECHARGEABLE BATTERIES?

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 RECHARGEABLE BATTERIES?

The FDA product code for RECHARGEABLE BATTERIES is FCO.

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: FCO)

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.

K946080PHYSIO CONTROL LIFEPAK 200 AUTO DEFIBRILLATORPortable Power Systems, Inc.K945870R&D PART NOS. 5490, 5541, 5358, 5497R & D Batteries, Inc.K944388R&D BATTERIES PART NOS. 5116, 5124, 5099, 5100R & D Batteries, Inc.K944348R&D BATTERIES, INC. PART NO. 5128, 5053, 5007R & D Batteries, Inc.K944389R&D BATTERIES PART NOS. 5111, 5112, 5065, 5153R & D Batteries, Inc.K945868R&D PART NOS. 5262, 5543, 5432, 5469R & D Batteries, Inc.

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.

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