The following data is part of a premarket notification filed by Armkel, Llc. with the FDA for Mono-latex (tm) Slide Test.
| Device ID | K862008 |
| 510k Number | K862008 |
| Device Name: | MONO-LATEX (TM) SLIDE TEST |
| Classification | System, Test, Infectious Mononucleosis |
| Applicant | ARMKEL, LLC. HALF ACRE RD. P.O. BOX 1001 Cranbury, NJ 08512 |
| Contact | S. C Kolakowsky |
| Correspondent | S. C Kolakowsky ARMKEL, LLC. HALF ACRE RD. P.O. BOX 1001 Cranbury, NJ 08512 |
| Product Code | KTN |
| CFR Regulation Number | 866.5640 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1986-05-27 |
| Decision Date | 1986-07-03 |