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FDA 510(k)

DEVICE FOR REPOSITIONING A BET PATIENT

K-Number: K813356 · 1982-02-10

Decision Date1982-02-10
Product CodeFNJ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DEVICE FOR REPOSITIONING A BET PATIENT is the device name listed in this FDA 510(k) record. The listed applicant is Ali-Oop Co., Inc.. It received FDA 510(k) clearance on 1982-02-10 under 510(k) number K813356. 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 DEVICE FOR REPOSITIONING A BET PATIENT?

DEVICE FOR REPOSITIONING A BET PATIENT is a medical device that received FDA 510(k) clearance on 1982-02-10. The listed applicant is Ali-Oop Co., Inc.. The 510(k) number is K813356.

When did DEVICE FOR REPOSITIONING A BET PATIENT receive FDA 510(k) clearance?

DEVICE FOR REPOSITIONING A BET PATIENT received FDA 510(k) clearance on 1982-02-10, under 510(k) number K813356.

Who is the listed applicant for DEVICE FOR REPOSITIONING A BET PATIENT?

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

What is the FDA product code for DEVICE FOR REPOSITIONING A BET PATIENT?

The FDA product code for DEVICE FOR REPOSITIONING A BET PATIENT 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.

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.

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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