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)

NEC-KRADLE BY VENCOR

K-Number: K844239 · 1984-11-19

ApplicantVencor
Decision Date1984-11-19
Product CodeHST
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

NEC-KRADLE BY VENCOR is the device name listed in this FDA 510(k) record. The listed applicant is Vencor. It received FDA 510(k) clearance on 1984-11-19 under 510(k) number K844239. The device is classified under product code HST. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEC-KRADLE BY VENCOR?

NEC-KRADLE BY VENCOR is a medical device that received FDA 510(k) clearance on 1984-11-19. The listed applicant is Vencor. The 510(k) number is K844239.

When did NEC-KRADLE BY VENCOR receive FDA 510(k) clearance?

NEC-KRADLE BY VENCOR received FDA 510(k) clearance on 1984-11-19, under 510(k) number K844239.

Who is the listed applicant for NEC-KRADLE BY VENCOR?

The FDA 510(k) record lists Vencor as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NEC-KRADLE BY VENCOR?

The FDA product code for NEC-KRADLE BY VENCOR is HST.

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

Related Devices (Code: HST)

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.

K162702Teeter Manual Inversion Table; Teeter Gravity Boots; Teeter Forward Rotation Decompression Device; Teeter Portable Decompression Device; Teeter Horizontal Decompression TableStl International, Inc.K110858LO-BAK TRAXRoland F Berthiaume, DCK984190BACK-ON-TRAC, MODEL 101BOTBack-On-Track, Inc.K872121K AND D HOME TRACTJoseph A. Kott, M.D.K870212ARTHROSCOPIC SHOULDER HOLDERDyonics, Inc.K870125EXTREMITY ELEVATOROrthopedic Systems, 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.

↑