The following data is part of a premarket notification filed by Espe Gmbh (us) with the FDA for Modified Visio-seal.
Device ID | K873069 |
510k Number | K873069 |
Device Name: | MODIFIED VISIO-SEAL |
Classification | Sealant, Pit And Fissure, And Conditioner |
Applicant | ESPE GMBH (US) 200 LAKE AVENUE (#205) Lake Worth, FL 33460 |
Contact | Harold A Opotow |
Correspondent | Harold A Opotow ESPE GMBH (US) 200 LAKE AVENUE (#205) Lake Worth, FL 33460 |
Product Code | EBC |
CFR Regulation Number | 872.3765 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1987-08-06 |
Decision Date | 1987-09-15 |