MPO ELISA TEST SYSTEM— 510(k) K961765
Substantially EquivalentImmunoprobe, Inc.
FDA 510(k) clearance K961765 for MPO ELISA TEST SYSTEM, Substantially Equivalent on 1996-08-19. Applicant: Immunoprobe, Inc.. Device class: 2.
Clearance details
- Applicant
- Immunoprobe, Inc.
- Product code
- Code MOB
- Device class
- Class 2
- Regulation
- 21 CFR 866.5660
- Advisory panel
- Immunology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Frederick, MD, US
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More clearances from Immunoprobe, Inc.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.