DEVICE FOR REPOSITIONING A BET PATIENT
K-Number: K813356 · 1982-02-10
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Device Summary
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
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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