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FDA 510(k)

BIO THERAPY PLUS

K-Number: K922205 · 1992-08-11

ApplicantSunrise Medical, Inc.
Decision Date1992-08-11
Product CodeFNM
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

BIO THERAPY PLUS is the device name listed in this FDA 510(k) record. The listed applicant is Sunrise Medical, Inc.. It received FDA 510(k) clearance on 1992-08-11 under 510(k) number K922205. The device is classified under product code FNM. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BIO THERAPY PLUS?

BIO THERAPY PLUS is a medical device that received FDA 510(k) clearance on 1992-08-11. The listed applicant is Sunrise Medical, Inc.. The 510(k) number is K922205.

When did BIO THERAPY PLUS receive FDA 510(k) clearance?

BIO THERAPY PLUS received FDA 510(k) clearance on 1992-08-11, under 510(k) number K922205.

Who is the listed applicant for BIO THERAPY PLUS?

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

What is the FDA product code for BIO THERAPY PLUS?

The FDA product code for BIO THERAPY PLUS is FNM.

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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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