ANTI-RESPIRATORY SYNCYTIAL VIRUS ANTIBODY TEST— 510(k) K882687
Substantially EquivalentGull Laboratories, Inc.
FDA 510(k) clearance K882687 for ANTI-RESPIRATORY SYNCYTIAL VIRUS ANTIBODY TEST, Substantially Equivalent on 1988-08-30. Applicant: Gull Laboratories, Inc.. Device class: 1.
Clearance details
- Applicant
- Gull Laboratories, Inc.
- Product code
- Code LKT
- Device class
- Class 1
- Regulation
- 21 CFR 866.3480
- Advisory panel
- Microbiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Salt Lake City, UT, US
Recent devices under product code LKT
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