HILL-ROM VIA STRETCHER (P1300 - P1303)
K-Number: K922808 · 1993-03-31
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Device Summary
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.
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
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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