FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
STREP CULTURETTE
K Number: K792201
·
Decision Nov 30, 1979
Classifications
1
FEI Numbers
3
Registration Numbers
3
Same Product Code
12
Applicant Total
2
Review Days
28
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Basic Information
- Device Name
- STREP CULTURETTE
- K Number
- K792201
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 866.2390
- Medical Specialty
- Microbiology
- Decision
- Substantially Equivalent
- Applicant
- Marion Health & Safety, Inc.
- Date Received
- November 2, 1979
- Decision Date
- November 30, 1979
- Product Code
- JSN
- 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 |
|---|---|---|---|
| JSN | Culture Media, Propagating Transport | FDA class 1 | Microbiology |
Similar 510(k) Clearances
Other 510(k) clearances with the same product code (JSN), ordered by most recent decision date.
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INPOUCH-TV POUCH
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AMIES TRANSPORT MEDIUM W/O CHARCOAL
FDA 510(k)
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Other Clearances by Marion Health & Safety, Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K800832 | VIRAL CULTURETTE HANK'S BAL. SALT SOL. | May 20, 1980 | Substantially Equivalent |