V.D.T.-GONORRHEA TEST KIT— 510(k) K840799
Substantially EquivalentM.G. Laboratories, Inc.
FDA 510(k) clearance K840799 for V.D.T.-GONORRHEA TEST KIT, Substantially Equivalent on 1984-06-07. Applicant: M.G. Laboratories, Inc.. Device class: 1.
Clearance details
- Applicant
- M.G. Laboratories, Inc.
- Product code
- Code LIO
- Device class
- Class 1
- Regulation
- 21 CFR 866.2900
- Advisory panel
- Microbiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Walker, MI, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.