MULTI-TEST
System, Delivery, Allergen And Vaccine
LINCOLN LABORATORIES, INC.
The following data is part of a premarket notification filed by Lincoln Laboratories, Inc. with the FDA for Multi-test.
Pre-market Notification Details
| Device ID | K760699 |
| 510k Number | K760699 |
| Device Name: | MULTI-TEST |
| Classification | System, Delivery, Allergen And Vaccine |
| Applicant | LINCOLN LABORATORIES, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | LDH |
| CFR Regulation Number | 510(k) Premarket Notification [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1976-09-22 |
| Decision Date | 1976-12-30 |
Trademark Results [MULTI-TEST]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 MULTI-TEST 85092912 4110868 Dead/Cancelled |
Koch Filter Corporation 2010-07-26 |
 MULTI-TEST 73644720 1492076 Live/Registered |
LINCOLN LABORATORIES, INC. 1987-02-12 |
 MULTI-TEST 73583098 not registered Dead/Abandoned |
LINCOLN DIAGNOSTICS, INC. 1986-02-18 |
 MULTI-TEST 73082621 1131107 Dead/Cancelled |
LINCOLN LABORATORIES, INC. 1976-04-05 |
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