The following data is part of a premarket notification filed by Bd Becton Dickinson Vacutainer Systems Preanalytic with the FDA for Anti-human Leu-3a (cd4) Fitc.
Device ID | K900802 |
510k Number | K900802 |
Device Name: | ANTI-HUMAN LEU-3A (CD4) FITC |
Classification | Counter, Differential Cell |
Applicant | BD BECTON DICKINSON VACUTAINER SYSTEMS PREANALYTIC 1 BECTON DR. Franklin Lakes, NJ 07417 -1880 |
Contact | J Arnsberger |
Correspondent | J Arnsberger BD BECTON DICKINSON VACUTAINER SYSTEMS PREANALYTIC 1 BECTON DR. Franklin Lakes, NJ 07417 -1880 |
Product Code | GKZ |
CFR Regulation Number | 864.5220 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1990-02-20 |
Decision Date | 1990-05-15 |
Device Identifier | submissionNumber | Supplement |
---|---|---|
00382903401338 | K900802 | 000 |