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510(k) K926044

MPM WET DRESSING (SALINE) by Mpm Medical., Inc. — Product Code KMF

K926044 is an FDA 510(k) premarket notification submitted by Mpm Medical., Inc. for the device "MPM WET DRESSING (SALINE)". The FDA issued a decision of Substantially Equivalent on April 8, 1993. The device falls under product code KMF (Bandage, Liquid), a Class I device regulated under 21 CFR 880.5090. Mpm Medical., Inc. has at least 8 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 8, 1993
Date Received
December 1, 1992
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 Mpm Medical., Inc.

  • K060340 — ORAMAGIC PLUS ORAL WOUND RINSE (May 10, 2006)
  • K024180 — ORAMAGICRX ORAL WOUND RINSE (March 14, 2003)
  • K020540 — REGENECARE WOUND GEL (November 1, 2002)
  • K992074 — MPM REGENECARE WOUND GEL (December 23, 1999)
  • K962160 — MPM HYDROGEL DRESSING (NON-STERILE) (June 26, 1996)
  • K952276 — MPM HYDROGEL DRESSING (June 30, 1995)
  • K942798 — MPM HYDROGEL (July 11, 1994)
  • K930560 — MPM HYDROGEL SATURATED DRESSING (July 8, 1993)

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