CURETTE SET, ANTRUM, COAKLEY
FDA 510(k) clearance K872609 · decided 1987-07-15
Clearance details
- K-number
- K872609
- Device name
- CURETTE SET, ANTRUM, COAKLEY
- Applicant
- Military Engineering, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1987-07-06
- Decision date
- 1987-07-15
- Days to decision
- 9 days
- Clearance type
- Traditional
- Product code
- KAP
- Device class
- 1
- Regulation number
- 874.4420
- Medical specialty
- Ear, Nose, Throat
- Advisory committee
- Ear, Nose, Throat
- Location
- Plymouth, IN, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.