FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
TISSUE CULTURE TUBES
K Number: K873889
·
Decision Nov 25, 1987
Classifications
1
FEI Numbers
31
Registration Numbers
31
Same Product Code
12
Applicant Total
3
Review Days
63
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Basic Information
- Device Name
- TISSUE CULTURE TUBES
- K Number
- K873889
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 864.2240
- Medical Specialty
- Hematology
- Decision
- Substantially Equivalent
- Applicant
- Nunc, Inc.
- Date Received
- September 23, 1987
- Decision Date
- November 25, 1987
- Product Code
- KJA
- 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 |
|---|---|---|---|
| KJA | Flask, Tissue Culture | FDA class 1 | Hematology |
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