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510(k) K973538

N-TERFACE by Winfield Laboratories, Inc. — Product Code MGP

K973538 is an FDA 510(k) premarket notification submitted by Winfield Laboratories, Inc. for the device "N-TERFACE". The FDA issued a decision of SN on December 16, 1997. The device falls under product code MGP (Dressing, Wound And Burn, Occlusive), a Class U device. Winfield Laboratories, Inc. has at least 3 other 510(k) clearances on record.

Clearance Details

Decision
SN ()
Decision Date
December 16, 1997
Date Received
September 18, 1997
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Dressing, Wound And Burn, Occlusive
Device Class
Class U
Regulation Number
Review Panel
SU
Submission Type

Other clearances by Winfield Laboratories, Inc.

  • K923602 — ABSORBENT PAD -- MODIFICATION (December 7, 1992)
  • K872069 — KONTOUR ULTRA SOFT SPONGE #SS144.50 (July 14, 1987)
  • K820198 — DERMA-AID (March 5, 1982)

Other clearances for product code MGP

  • K012995 — COLLATEK SHEET (October 25, 2001)
  • K012997 — COLLATEK FOAM (October 25, 2001)
  • K001508 — LASERSKIN DRESSING (July 25, 2001)
  • K990079 — FASTSEAL CHEST WOUND DRESSING (December 23, 1999)
  • K991214 — SIMPLICARE TRANSPARENT WOUND DRESSING (October 14, 1999)
  • K992302 — DERMAPHYLYX SKIN PROTECTORS, PROTECT IT SKIN PROTECTORS (September 14, 1999)
  • K992005 — GILTECH PLUS TRANSPARENT DRESSING (September 3, 1999)
  • K990875 — DERMAPHYLYX FILM WOUND DRESSING AND HEALIAN FILM WOUND DRESSING (May 27, 1999)
  • K990438 — DERMAFLEX WOUND DRESSING, DERMAFLEX FOAM WOUND DRESSING, HEALIAFLEX WOUND DRESSI (March 25, 1999)
  • K984371 — MEPITEL NON ADHERENT SILICONE DRESSING (March 3, 1999)

FDA data resources