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BIO THERAPY PLUS

K922205 Class II Traditional
Decision Date
1992-08-11
Sponsor / Applicant
Sunrise Medical, Inc.

Technical Specification

510(k) Submission ID K922205
Product Code FNM
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5550
Decision Date 1992-08-11
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BIO THERAPY PLUS received FDA 510(k) clearance under submission number K922205, sponsored by Sunrise Medical, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 1992-08-11.

Classification & Regulation

This clearance is catalogued under FDA product code FNM and 21 CFR 880.5550, within the General Hospital review panel as a Class II device.