The following data is part of a premarket notification filed by Scientific Pharmaceuticals, Inc. with the FDA for Unirest Pl, Ante./post. Restorative, Paste/liquid.
Device ID | K884351 |
510k Number | K884351 |
Device Name: | UNIREST PL, ANTE./POST. RESTORATIVE, PASTE/LIQUID |
Classification | Material, Tooth Shade, Resin |
Applicant | SCIENTIFIC PHARMACEUTICALS, INC. 1828 EVERGREEN ST. Duarte, CA 91010 |
Contact | Jan A Orlowski |
Correspondent | Jan A Orlowski SCIENTIFIC PHARMACEUTICALS, INC. 1828 EVERGREEN ST. Duarte, CA 91010 |
Product Code | EBF |
CFR Regulation Number | 872.3690 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1988-10-14 |
Decision Date | 1988-12-28 |