The following data is part of a premarket notification filed by Ttl Medical with the FDA for Derma Seal.
Device ID | K952702 |
510k Number | K952702 |
Device Name: | DERMA SEAL |
Classification | Strip, Adhesive, Closure, Skin |
Applicant | TTL MEDICAL 10537 LEXINGTON DR. KNOXVILLE, TN 37932 |
Contact | H. CLAY WILSON |
Correspondent | H. CLAY WILSON TTL MEDICAL 10537 LEXINGTON DR. KNOXVILLE, TN 37932 |
Product Code | FPX |
CFR Regulation Number | 880.5240 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1995-06-13 |
Decision Date | 1995-06-28 |