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FDA 510(k)

HILL-ROM VIA STRETCHER (P1300 - P1303)

K-Number: K922808 · 1993-03-31

Decision Date1993-03-31
Product CodeFPO
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

HILL-ROM VIA STRETCHER (P1300 - P1303) is the device name listed in this FDA 510(k) record. The listed applicant is Hill-Rom, Inc.. It received FDA 510(k) clearance on 1993-03-31 under 510(k) number K922808. The device is classified under product code FPO. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HILL-ROM VIA STRETCHER (P1300 - P1303)?

HILL-ROM VIA STRETCHER (P1300 - P1303) is a medical device that received FDA 510(k) clearance on 1993-03-31. The listed applicant is Hill-Rom, Inc.. The 510(k) number is K922808.

When did HILL-ROM VIA STRETCHER (P1300 - P1303) receive FDA 510(k) clearance?

HILL-ROM VIA STRETCHER (P1300 - P1303) received FDA 510(k) clearance on 1993-03-31, under 510(k) number K922808.

Who is the listed applicant for HILL-ROM VIA STRETCHER (P1300 - P1303)?

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

What is the FDA product code for HILL-ROM VIA STRETCHER (P1300 - P1303)?

The FDA product code for HILL-ROM VIA STRETCHER (P1300 - P1303) is FPO.

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.

Other records listing Hill-Rom, 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.

View all 34 devices →

Related Devices (Code: FPO)

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.

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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