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FDA 510(k)

PNEUMATIC/ELECTRIC/HYDRAULIC BED

K-Number: K831821 · 1983-08-08

ApplicantG.W. Healthcare, Inc.
Decision Date1983-08-08
Product CodeFNL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PNEUMATIC/ELECTRIC/HYDRAULIC 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 1983-08-08 under 510(k) number K831821. The device is classified under product code FNL. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PNEUMATIC/ELECTRIC/HYDRAULIC BED?

PNEUMATIC/ELECTRIC/HYDRAULIC BED is a medical device that received FDA 510(k) clearance on 1983-08-08. The listed applicant is G.W. Healthcare, Inc.. The 510(k) number is K831821.

When did PNEUMATIC/ELECTRIC/HYDRAULIC BED receive FDA 510(k) clearance?

PNEUMATIC/ELECTRIC/HYDRAULIC BED received FDA 510(k) clearance on 1983-08-08, under 510(k) number K831821.

Who is the listed applicant for PNEUMATIC/ELECTRIC/HYDRAULIC 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 PNEUMATIC/ELECTRIC/HYDRAULIC BED?

The FDA product code for PNEUMATIC/ELECTRIC/HYDRAULIC BED is FNL.

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.

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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.

K830559HEALTHCARE MODEL #175/176 BED SERIESK812600GER 540, GER 541 MANUAL BED

Related Devices (Code: FNL)

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.

K202964iBed Wireless with iBed MobileStryker CorporationK103536IBED WIRELESS WITH IBED AWARENESSStryker CorporationK982783VAIL 1000 ENCLOSED BEDVail Products, Inc.K974296MODEL 720 SERIES FULL/SEMI ELECTRIC BED 1120 FULL ELECTRIC BEDInvacare Corp.K974254BENEFIT B3--- SERIESM.C. Healthcare Products, Inc.K972115VOLKER HOSPITAL BED, MODEL K960Volker Healthcare, 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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