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BRADY MEDICAL PRODUCTS HYSORB(TM) WOUND DRESSING

K936052 Class I Traditional
Decision Date
1994-03-07
Sponsor / Applicant
Brady Medical Products Co.

Technical Specification

510(k) Submission ID K936052
Product Code KMF
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5090
Decision Date 1994-03-07
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BRADY MEDICAL PRODUCTS HYSORB(TM) WOUND DRESSING received FDA 510(k) clearance under submission number K936052, sponsored by Brady Medical Products Co.. 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 1994-03-07.

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.