RAMPIPELLA, SINGE PORT (720196) & WEDGE-SHAPED PORT (720217)— 510(k) K991895
Substantially EquivalentRi Mos. S.R.L.
FDA 510(k) clearance K991895 for RAMPIPELLA, SINGE PORT (720196) & WEDGE-SHAPED PORT (720217), Substantially Equivalent on 1999-08-12. Applicant: Ri Mos. S.R.L.. Device class: 2.
Clearance details
- Applicant
- Ri Mos. S.R.L.
- Product code
- Code HHK
- Device class
- Class 2
- Regulation
- 21 CFR 884.1175
- Advisory panel
- Obstetrics/Gynecology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Concord, MA, US
Recent devices under product code HHK
view allMore clearances from Ri Mos. S.R.L.
view all- K992926 — GINRAM ENDOCIC SINGLE OVAL PORT (MODEL NO. 720195)
- K991827 — GINRAM SPECUVAG, GINRAM SPECUVAG AS, GINRAM CUSCOVAG, MODELS 720101, 720102, 720103, 720179, 720227, 720043
- K983897 — CERVICAL ANESTHESIA NEEDLE, CONTRACERVICAL ANESTHESIA NEEDLE, MODEL #'S 720209 30GAU X 4 MM, 720210 30GAU X 6MM, 720208G
Data sourced from openFDA. This site is unofficial and independent of the FDA.