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FDA 510(k)

VOLKER HOSPITAL BED, MODEL K960

K-Number: K972115 · 1997-08-29

ApplicantVolker Healthcare, Inc.
Decision Date1997-08-29
Product CodeFNL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

VOLKER HOSPITAL BED, MODEL K960 is the device name listed in this FDA 510(k) record. The listed applicant is Volker Healthcare, Inc.. It received FDA 510(k) clearance on 1997-08-29 under 510(k) number K972115. 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 VOLKER HOSPITAL BED, MODEL K960?

VOLKER HOSPITAL BED, MODEL K960 is a medical device that received FDA 510(k) clearance on 1997-08-29. The listed applicant is Volker Healthcare, Inc.. The 510(k) number is K972115.

When did VOLKER HOSPITAL BED, MODEL K960 receive FDA 510(k) clearance?

VOLKER HOSPITAL BED, MODEL K960 received FDA 510(k) clearance on 1997-08-29, under 510(k) number K972115.

Who is the listed applicant for VOLKER HOSPITAL BED, MODEL K960?

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

What is the FDA product code for VOLKER HOSPITAL BED, MODEL K960?

The FDA product code for VOLKER HOSPITAL BED, MODEL K960 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 Volker 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.

K946208VOLKER NURSING BED MODEL 2080E & 2090E

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.K971546SOMA 900 TRANSPORT BEDNova Technologies, Inc.

Official Source

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

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