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DOCTOR DOWN --RESCUE WRAP

K932539 Class I Traditional
Decision Date
1993-11-02
Sponsor / Applicant
Three Dog Down

Technical Specification

510(k) Submission ID K932539
Product Code KME
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6060
Decision Date 1993-11-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DOCTOR DOWN --RESCUE WRAP received FDA 510(k) clearance under submission number K932539, sponsored by Three Dog Down. 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 1993-11-02.

Classification & Regulation

This clearance is catalogued under FDA product code KME and 21 CFR 880.6060, within the General Hospital review panel as a Class I device.