The following data is part of a premarket notification filed by Acme United Corp. with the FDA for Lyofoam Extra.
Device ID | K952565 |
510k Number | K952565 |
Device Name: | LYOFOAM EXTRA |
Classification | Bandage, Liquid |
Applicant | ACME UNITED CORP. 75 KINGS HWY. CUT-OFF Fairfield, CT 06430 |
Contact | Thomas E Flynn |
Correspondent | Thomas E Flynn ACME UNITED CORP. 75 KINGS HWY. CUT-OFF Fairfield, CT 06430 |
Product Code | KMF |
CFR Regulation Number | 880.5090 [🔎] |
Decision | Substantially Equivalent For Some Indications (SN) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1995-06-02 |
Decision Date | 1995-11-14 |