The following data is part of a premarket notification filed by Acrymed, Inc. with the FDA for Acrynoodles Absorbent Wound Dressing.
Device ID | K962851 |
510k Number | K962851 |
Device Name: | ACRYNOODLES ABSORBENT WOUND DRESSING |
Classification | Dressing, Wound And Burn, Hydrogel W/drug And/or Biologic |
Applicant | ACRYMED, INC. 12232 S.W. GARDEN PL. Portland, OR 97223 |
Contact | Bruce Gibbins |
Correspondent | Bruce Gibbins ACRYMED, INC. 12232 S.W. GARDEN PL. Portland, OR 97223 |
Product Code | MGQ |
CFR Regulation Number | 510(k) Premarket Notification [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1996-07-22 |
Decision Date | 1996-09-06 |
Summary: | summary |