CERVICAL ANESTHESIA NEEDLE, CONTRACERVICAL ANESTHESIA NEEDLE, MODEL #'S 720209 30GAU X 4 MM, 720210 30GAU X 6MM, 720208G— 510(k) K983897
Substantially EquivalentRi Mos. S.R.L.
FDA 510(k) clearance K983897 for CERVICAL ANESTHESIA NEEDLE, CONTRACERVICAL ANESTHESIA NEEDLE, MODEL #'S 720209 30GAU X 4 MM, 720210 30GAU X 6MM, 720208G, Substantially Equivalent on 1999-02-01. Applicant: Ri Mos. S.R.L.. Device class: 2.
Clearance details
- Applicant
- Ri Mos. S.R.L.
- Product code
- Code HEE
- Device class
- Class 2
- Regulation
- 21 CFR 884.5100
- Advisory panel
- Obstetrics/Gynecology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Concord, MA, US
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