The following data is part of a premarket notification filed by Bd Becton Dickinson Vacutainer Systems Preanalytic with the FDA for Becton Dickinson Syringe.
Device ID | K992734 |
510k Number | K992734 |
Device Name: | BECTON DICKINSON SYRINGE |
Classification | Syringe, Antistick |
Applicant | BD BECTON DICKINSON VACUTAINER SYSTEMS PREANALYTIC 1 BECTON DRIVE, BLDG 2, MAIL CODE 226 Franklin Lakes, NJ 07417 |
Contact | Greg Morgan |
Correspondent | Greg Morgan BD BECTON DICKINSON VACUTAINER SYSTEMS PREANALYTIC 1 BECTON DRIVE, BLDG 2, MAIL CODE 226 Franklin Lakes, NJ 07417 |
Product Code | MEG |
CFR Regulation Number | 880.5860 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1999-08-13 |
Decision Date | 1999-10-01 |
Summary: | summary |
Device Identifier | submissionNumber | Supplement |
---|---|---|
50382903059510 | K992734 | 000 |
50382903059046 | K992734 | 000 |
50382903059053 | K992734 | 000 |
50382903059060 | K992734 | 000 |
50382903059077 | K992734 | 000 |
50382903059084 | K992734 | 000 |
50382903059091 | K992734 | 000 |
50382903059244 | K992734 | 000 |
50382903059459 | K992734 | 000 |
50382903059466 | K992734 | 000 |
50382903059503 | K992734 | 000 |
20612479262786 | K992734 | 000 |