FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
TISSUE CULTURE/BACTERIOLOGICAL PETRI DISHES
K Number: K871483
·
Decision Apr 29, 1987
Classifications
1
FEI Numbers
69
Registration Numbers
69
Same Product Code
7
Applicant Total
2
Review Days
14
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Basic Information
- Device Name
- TISSUE CULTURE/BACTERIOLOGICAL PETRI DISHES
- K Number
- K871483
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 864.2240
- Medical Specialty
- Hematology
- Decision
- Substantially Equivalent
- Applicant
- Isratech Marketing Corp.
- Date Received
- April 15, 1987
- Decision Date
- April 29, 1987
- Product Code
- KIZ
- Advisory Committee
- Hematology
- Review Advisory Committee
- PA
- 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 |
|---|---|---|---|
| KIZ | Dish, Tissue Culture | FDA class 1 | Hematology |
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Other Clearances by Isratech Marketing Corp.
| K Number | Device Name | ||
|---|---|---|---|
| K896165 | STERILE HYPOALLERGENIC SURGEONS' GLOVES | Nov 22, 1989 | Substantially Equivalent |