Becton Dickinson Vacutainer Systems
Franklin Lake, NJ, US
Becton Dickinson Vacutainer Systems appears in FDA device records in Franklin Lake, NJ. FDA records list 15 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.
FDA records held for this company
- 510(k) clearances
- 15
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 15 510(k) clearances for Becton Dickinson Vacutainer Systems between 1995 and 2000. The busiest year on record is 1998, with 5. The most recent is 2000, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1995 | 4 |
| 1996 | 1 |
| 1997 | 1 |
| 1998 | 5 |
| 1999 | 3 |
| 2000 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K002456 | MICROTAINER BRAND SODIUM FLUORIDE/EDTA TUBE WITH MICROGARD CLOSURE, MODEL 365992 | JKA | Substantially Equivalent | |
| K991702 | MICROTAINER BRAND CHEMISTRY TUBES WITH MICROGARD CLOSURE, MODEL 365965, 365985, 365963, 365967, 36578 | JKA | Substantially Equivalent | |
| K991088 | VACUTAINER BRAND MULTIPLE SAMPLE LUER ADAPTER, BLOOD COLLECTION SETS AND SAFETY-LOK BLOOD COLLECTION, SAFETY BLOOD COLLE | JKA | Substantially Equivalent | |
| K991120 | VACUTAINER BRAND CTAD TUBE (MULTIPLE) | JKA | Substantially Equivalent | |
| K982541 | VACUTAINER BRAND ECLIPSE BLOOD COLLECTION NEEDLE, MODELS# 368607 & 368608 | FMI | Substantially Equivalent | |
| K982922 | VACUTAINER BRAND BLOOD COLLECTION SYRINGE | JKA | Substantially Equivalent | |
| K981013 | VACUTAINER PLUS TUBE WITH EDTA ANTICOAGULANT ANDD VACUTAINER PLUS SERUM TUBE | JKA | Substantially Equivalent for Some Indications | |
| K972075 | VACUTAINER BRAND PPT PLASMA PREPARATION TUBE | PJE | Substantially Equivalent | |
| K980098 | VACUTAINER BRAND PRONTO NEEDLES HOLDER | JKA | Substantially Equivalent | |
| K971449 | VACUTAINER BRAND PLUS TUBE WITH EDTA ANTICOAGULANT(MULTIPLE) | GIM | Substantially Equivalent | |
| K960250 | VACUTAINER BRAND PLUS SERUM & SST TUBES | JKA | Substantially Equivalent | |
| K954592 | VACUTAINER BRAND PST PLASMA SEPARATION TUBE | JKA | Substantially Equivalent | |
| K953994 | SEDITAINER* ERYTHROCYTE SEDIMENTATION RATE (ESR) SYSTEM | JKA | Substantially Equivalent | |
| K953463 | VACUTAINER PLUS TUBES | JKA | Substantially Equivalent | |
| K951886 | LOK-ON NEEDLE DISPOSAL SYSTEM | GIM | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
Recall records
No recall records for this company in the ingested FDA data.
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain