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ALTA DRESSING FRAME

K926380 Class I Traditional
Decision Date
1993-08-06
Sponsor / Applicant
Alta Medical Products, Inc.

Technical Specification

510(k) Submission ID K926380
Product Code KMF
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5090
Decision Date 1993-08-06
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ALTA DRESSING FRAME received FDA 510(k) clearance under submission number K926380, sponsored by Alta Medical Products, 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 1993-08-06.

Classification & Regulation

This clearance is catalogued under FDA product code KMF and 21 CFR 880.5090, within the General Hospital review panel as a Class I device.