The following data is part of a premarket notification filed by Clinical Supply with the FDA for Patient Examination Gloves (latex).
Device ID | K891665 |
510k Number | K891665 |
Device Name: | PATIENT EXAMINATION GLOVES (LATEX) |
Classification | Latex Patient Examination Glove |
Applicant | CLINICAL SUPPLY 7969 CINCINNATI DAYTON RD. West Chester, OH 45069 |
Contact | Mark Carnahan |
Correspondent | Mark Carnahan CLINICAL SUPPLY 7969 CINCINNATI DAYTON RD. West Chester, OH 45069 |
Product Code | LYY |
CFR Regulation Number | 880.6250 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1989-03-20 |
Decision Date | 1989-07-31 |