FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
STREP-ID PLATE
K Number: K811422
·
Decision Jun 18, 1981
Classifications
1
FEI Numbers
30
Registration Numbers
30
Same Product Code
284
Applicant Total
24
Review Days
29
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Basic Information
- Device Name
- STREP-ID PLATE
- K Number
- K811422
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 866.2360
- Medical Specialty
- Microbiology
- Decision
- Substantially Equivalent
- Applicant
- Carr-Scarborough Microbiologicals, Inc.
- Date Received
- May 20, 1981
- Decision Date
- June 18, 1981
- Product Code
- JSI
- 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 |
|---|---|---|---|
| JSI | Culture Media, Selective And Differential | FDA class 1 | Microbiology |
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Other Clearances by Carr-Scarborough Microbiologicals, Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K944554 | BRAIN HEART INFUSION AGAR | Oct 4, 1994 | Substantially Equivalent |
| K941985 | MUELLER HINTON AGAR W/OXACILLIN | Aug 24, 1994 | Substantially Equivalent |
| K905472 | LAP DISCS | Feb 27, 1991 | Substantially Equivalent |
| K905666 | M. CAT. BUTYRATE DISC | Feb 26, 1991 | Substantially Equivalent |
| K891476 | C. ALBICANS SCREEN | Apr 12, 1989 | Substantially Equivalent |
| K882630 | PRO DISCS | Feb 16, 1989 | Substantially Equivalent |
| K882636 | ALN DISCS | Feb 16, 1989 | Substantially Equivalent |
| K863216 | NEIS NZY | Sep 15, 1986 | Substantially Equivalent |
| K860301 | RAPID GLUTAMIC ACID DECARBOXYLASE (GDC) MICROTUBE | Feb 6, 1986 | Substantially Equivalent |
| K860302 | PYR DISCS | Feb 5, 1986 | Substantially Equivalent |