FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
PACT SUPPLEMENT
K Number: K810591
·
Decision Mar 20, 1981
Classifications
1
FEI Numbers
15
Registration Numbers
15
Same Product Code
69
Applicant Total
632
Review Days
15
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Basic Information
- Device Name
- PACT SUPPLEMENT
- K Number
- K810591
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 866.2450
- Medical Specialty
- Microbiology
- Decision
- Substantially Equivalent
- Applicant
- Bd Becton Dickinson Vacutainer Systems Preanalytic
- Date Received
- March 5, 1981
- Decision Date
- March 20, 1981
- Product Code
- JSK
- Advisory Committee
- Microbiology
- Review Advisory Committee
- MI
- Third Party
- N
Classifications
This FDA 510(k) entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| JSK | Supplement, Culture Media | FDA class 1 | Microbiology |
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|---|---|---|---|
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| K002938 | B-D ULTRA-FINE III PEN NEEDLE; MODEL 31G X 3/16 | Nov 29, 2000 | Substantially Equivalent |
| K001364 | BD DIRECTIGEN FLU A+B | Jun 28, 2000 | Substantially Equivalent |
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| K000829 | GATIFLOXACIN, 5 UG, BBL SENSI-DISC | Apr 13, 2000 | Substantially Equivalent |
| K993186 | SYNERCID, 15 UG, BBL SENSI-DISC | Nov 3, 1999 | Substantially Equivalent |
| K992734 | BECTON DICKINSON SYRINGE | Oct 1, 1999 | Substantially Equivalent |
| K991551 | VACUTAINER BRAND SODIUM CITRATE PEDIATRIC TUBE | Sep 23, 1999 | Substantially Equivalent |