The following data is part of a premarket notification filed by Orasure Technologies, Inc. with the FDA for Histofreezer/ 17% Salicylic Acid-verruca Plantaris.
Device ID | K980739 |
510k Number | K980739 |
Device Name: | HISTOFREEZER/ 17% SALICYLIC ACID-VERRUCA PLANTARIS |
Classification | Unit, Cryosurgical, Accessories |
Applicant | ORASURE TECHNOLOGIES, INC. 1745 EATON AVE. Bethlehem, PA 18018 -1799 |
Contact | R. Sam Niedbala |
Correspondent | R. Sam Niedbala ORASURE TECHNOLOGIES, INC. 1745 EATON AVE. Bethlehem, PA 18018 -1799 |
Product Code | GEH |
CFR Regulation Number | 878.4350 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1998-02-25 |
Decision Date | 1998-05-26 |