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FDA 510(k)

GER 540, GER 541 MANUAL BED

K-Number: K812600 · 1981-09-23

ApplicantG.W. Healthcare, Inc.
Decision Date1981-09-23
Product CodeFNJ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

GER 540, GER 541 MANUAL BED is the device name listed in this FDA 510(k) record. The listed applicant is G.W. Healthcare, Inc.. It received FDA 510(k) clearance on 1981-09-23 under 510(k) number K812600. The device is classified under product code FNJ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GER 540, GER 541 MANUAL BED?

GER 540, GER 541 MANUAL BED is a medical device that received FDA 510(k) clearance on 1981-09-23. The listed applicant is G.W. Healthcare, Inc.. The 510(k) number is K812600.

When did GER 540, GER 541 MANUAL BED receive FDA 510(k) clearance?

GER 540, GER 541 MANUAL BED received FDA 510(k) clearance on 1981-09-23, under 510(k) number K812600.

Who is the listed applicant for GER 540, GER 541 MANUAL BED?

The FDA 510(k) record lists G.W. Healthcare, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for GER 540, GER 541 MANUAL BED?

The FDA product code for GER 540, GER 541 MANUAL BED is FNJ.

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 G.W. Healthcare, 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.

K831821PNEUMATIC/ELECTRIC/HYDRAULIC BEDK830559HEALTHCARE MODEL #175/176 BED SERIES

Related Devices (Code: FNJ)

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.

K934298KING KRIBNoritage, Inc.K892877CRADLE, HOSPITAL BED CLOTHINGWarsaw Orthopedic, Inc.K885241BED, ADJUSTABLE, HOSPITAL, FOLDING, FIELD, W/O MATKing Mfg. Co.K884542SIC 3999 FOLDING ADJUSTABLE HOSPITAL BEDCommercial Products & Engineering Co.K881725ENVIROTENT (BED)Envirotents, Inc.K881961MSI STANDARD BED MODELS: L1097-64 AND L1085-64Med Service, 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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