CERVICAL SPATULA— 510(k) K811548
Substantially EquivalentProcedure Products, Inc.
FDA 510(k) clearance K811548 for CERVICAL SPATULA, Substantially Equivalent on 1981-06-23. Applicant: Procedure Products, Inc.. Device class: 2.
Clearance details
- Applicant
- Procedure Products, Inc.
- Product code
- Code HHT
- Device class
- Class 2
- Regulation
- 21 CFR 884.4530
- Advisory panel
- Obstetrics/Gynecology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
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