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510(k) K936052

BRADY MEDICAL PRODUCTS HYSORB(TM) WOUND DRESSING by Brady Medical Products Co. — Product Code KMF

K936052 is an FDA 510(k) premarket notification submitted by Brady Medical Products Co. for the device "BRADY MEDICAL PRODUCTS HYSORB(TM) WOUND DRESSING". The FDA issued a decision of SN on March 7, 1994. The device falls under product code KMF (Bandage, Liquid), a Class I device regulated under 21 CFR 880.5090. Brady Medical Products Co. has at least 4 other 510(k) clearances on record.

Clearance Details

Decision
SN ()
Decision Date
March 7, 1994
Date Received
December 20, 1993
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Bandage, Liquid
Device Class
Class I
Regulation Number
880.5090
Review Panel
SU
Submission Type

Other clearances by Brady Medical Products Co.

  • K945832 — BRADY MEDICAL PRODUCTS TRANSCORBENT AND THINSITE TOPICAL BORDER WOUND DRESSINGS (March 1, 1995)
  • K941019 — BRADY MEDICAL PRODUCTS TRANSORBENTS WOUND DRESSING (May 4, 1994)
  • K935848 — BRADY MEDICAL PRODUCTS TRANSORB WOUND DRESSING (February 15, 1994)
  • K922666 — TRANSORB(TM) ULCER & WOUND DRESSING (November 23, 1992)

Other clearances for product code KMF

  • K241916 — TearRepair Liquid Skin Protectant (September 27, 2024)
  • K182733 — Rochal Bioshield Silicone Film (June 27, 2019)
  • K171148 — Aleo BME Liquid Bandage (January 12, 2018)
  • K153571 — Cavilon Advanced High Endurance Skin Protectant (August 23, 2016)
  • K160684 — Atteris No-Sting Skin Protectant (July 26, 2016)
  • K131384 — KERICURE ADVANCED LIQUID BANDAGE, NATURAL SEAL LIQUID BANDAGE, LIQUID BANDAGE (August 7, 2014)
  • K133443 — MARATHON NO STING LIQUID SKIN PROTECTANT (July 10, 2014)
  • K120059 — LIQUID BANDAGE (May 17, 2012)
  • K092712 — SKIN BARRIER FILM (February 23, 2010)
  • K083087 — ECOCEL (August 7, 2009)

FDA data resources