The following data is part of a premarket notification filed by Gac Intl., Inc. with the FDA for Orthodontic Elastomer.
Device ID | K932319 |
510k Number | K932319 |
Device Name: | ORTHODONTIC ELASTOMER |
Classification | Band, Elastic, Orthodontic |
Applicant | GAC INTL., INC. 185 OVAL DR. Central Islip, NY 11722 |
Contact | Ernest Bohn |
Correspondent | Ernest Bohn GAC INTL., INC. 185 OVAL DR. Central Islip, NY 11722 |
Product Code | ECI |
CFR Regulation Number | 872.5410 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1993-05-11 |
Decision Date | 1993-09-20 |