GINRAM ENDOCIC SINGLE OVAL PORT (MODEL NO. 720195)— 510(k) K992926
Substantially EquivalentRi Mos. S.R.L.
FDA 510(k) clearance K992926 for GINRAM ENDOCIC SINGLE OVAL PORT (MODEL NO. 720195), Substantially Equivalent on 1999-10-26. 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- K991895 — RAMPIPELLA, SINGE PORT (720196) & WEDGE-SHAPED PORT (720217)
- 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.