The following data is part of a premarket notification filed by Dynatech Laboratories, Inc. with the FDA for Multi-channel Micropipettes.
Device ID | K862802 |
510k Number | K862802 |
Device Name: | MULTI-CHANNEL MICROPIPETTES |
Classification | Device, Microtiter Diluting/dispensing |
Applicant | DYNATECH LABORATORIES, INC. 14340 SULLYFIELD CIRCLE Chantilly, VA 22021 |
Contact | Heidi E Chandonnet |
Correspondent | Heidi E Chandonnet DYNATECH LABORATORIES, INC. 14340 SULLYFIELD CIRCLE Chantilly, VA 22021 |
Product Code | JTC |
CFR Regulation Number | 866.2500 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1986-07-22 |
Decision Date | 1986-08-01 |