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510(k) K992032

ACRY ISLAND BORDER DRESSING, MODELS 2031, 2032, 2033 by Acrymed, Inc. — Product Code KMF

K992032 is an FDA 510(k) premarket notification submitted by Acrymed, Inc. for the device "ACRY ISLAND BORDER DRESSING, MODELS 2031, 2032, 2033". The FDA issued a decision of Substantially Equivalent on August 19, 1999. The device falls under product code KMF (Bandage, Liquid), a Class I device regulated under 21 CFR 880.5090. Acrymed, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 19, 1999
Date Received
June 16, 1999
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 Acrymed, Inc.

  • K091354 — ACRYDERM SILVER ANTIMICROBIAL FOAM WOUND DRESSING (October 21, 2009)
  • K083103 — ACRYDERM ANTIMICROBIAL SILVER GEL WOUND DRESSING MODEL #B (February 26, 2009)
  • K082459 — ACRYDERM ABSORBENT OXYGEN DRESSING (September 19, 2008)
  • K070333 — ACRYDERM SILVER ANTIMICROBIAL OTC WOUND GEL (July 10, 2007)
  • K061232 — ACRYDERM SILVER ANTIMICROBIAL THIN FILM, MODEL 2006 (October 6, 2006)
  • K011994 — ACRYDERM SILVER ANTTIMICROBIAL WOUND GEL MODEL# A-002101 (November 8, 2001)
  • K012116 — ACRYDERM SILVER ANTIMICROBIAL PERFORATED WOUND DRESSING (September 12, 2001)
  • K002909 — ACRYDERM SILVER ANTIMICROBIAL STRANDS MODEL A-020103 (October 13, 2000)
  • K002599 — MODIFICATION TO ACRYDERM SILVER ANTIMICROBIAL WOUND DRESSING, MODELS 1041, 1042, (September 21, 2000)
  • K991818 — ACRYDERM SILVER ANTI-MICROBIAL WOUND DRESSING, MODELS 1041, 1042, 1043, 1044, 10 (April 17, 2000)

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