MYCOPLASMA IGG ELISA TEST SYSTEM— 510(k) K971393
Substantially EquivalentImmunoprobe, Inc.
FDA 510(k) clearance K971393 for MYCOPLASMA IGG ELISA TEST SYSTEM, Substantially Equivalent on 1997-07-14. Applicant: Immunoprobe, Inc.. Device class: 1.
Clearance details
- Applicant
- Immunoprobe, Inc.
- Product code
- Code LJZ
- Device class
- Class 1
- Regulation
- 21 CFR 866.3375
- Advisory panel
- Microbiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Frederick, MD, US
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More clearances from Immunoprobe, Inc.
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