FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
ABBOTT TESTPACK RSV
K Number: K874127
·
Decision May 6, 1988
Classifications
1
FEI Numbers
35
Registration Numbers
35
Same Product Code
31
Applicant Total
883
Review Days
206
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Basic Information
- Device Name
- ABBOTT TESTPACK RSV
- K Number
- K874127
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 866.3480
- Medical Specialty
- Microbiology
- Decision
- Substantially Equivalent
- Applicant
- Abbott Laboratories
- Date Received
- October 13, 1987
- Decision Date
- May 6, 1988
- Product Code
- GQG
- 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 |
|---|---|---|---|
| GQG | Antigen, Cf (Including Cf Controls), Respiratory Syncytial Virus | FDA class 1 | Microbiology |
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