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FDA 510(k)

ANAGO DISP., ALL PURPOSE PATIENT REST.

K-Number: K800197 · 1980-02-26

ApplicantAnago, Inc.
Decision Date1980-02-26
Product CodeFQM
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ANAGO DISP., ALL PURPOSE PATIENT REST. is the device name listed in this FDA 510(k) record. The listed applicant is Anago, Inc.. It received FDA 510(k) clearance on 1980-02-26 under 510(k) number K800197. The device is classified under product code FQM. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANAGO DISP., ALL PURPOSE PATIENT REST.?

ANAGO DISP., ALL PURPOSE PATIENT REST. is a medical device that received FDA 510(k) clearance on 1980-02-26. The listed applicant is Anago, Inc.. The 510(k) number is K800197.

When did ANAGO DISP., ALL PURPOSE PATIENT REST. receive FDA 510(k) clearance?

ANAGO DISP., ALL PURPOSE PATIENT REST. received FDA 510(k) clearance on 1980-02-26, under 510(k) number K800197.

Who is the listed applicant for ANAGO DISP., ALL PURPOSE PATIENT REST.?

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

What is the FDA product code for ANAGO DISP., ALL PURPOSE PATIENT REST.?

The FDA product code for ANAGO DISP., ALL PURPOSE PATIENT REST. is FQM.

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Other records listing Anago, Inc. as applicant

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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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