QUIK-CHECK OVULATION PREDICTOR— 510(k) K012252
Substantially EquivalentACON Laboratories, Inc.
FDA 510(k) clearance K012252 for QUIK-CHECK OVULATION PREDICTOR, Substantially Equivalent on 2001-08-24. Applicant: ACON Laboratories, Inc.. Device class: 1.
Clearance details
- Applicant
- ACON Laboratories, Inc.
- Product code
- Code CEP
- Device class
- Class 1
- Regulation
- 21 CFR 862.1485
- Advisory panel
- Clinical Chemistry
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Beverly, MA, US
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