OVAMED INTRAUTERINE ACCESS CATHETER— 510(k) K931534

Name: FDA 510(k) clearance K931534
Creator: U.S. Food and Drug Administration
Published: 1995-07-28

Substantially Equivalent

Ovamed Corp.

FDA 510(k) clearance K931534 for OVAMED INTRAUTERINE ACCESS CATHETER, Substantially Equivalent on 1995-07-28. Applicant: Ovamed Corp.. Device class: 2.

Clearance details

Applicant: Ovamed Corp.
Product code: Code MOV
Device class: Class 2
Regulation: 21 CFR 884.4530
Advisory panel: Obstetrics/Gynecology
Date received: 1993-03-29
Decision date: 1995-07-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Sunnyvale, CA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code MOV

view all

K180552 — Modified Novy Cornual Cannulation Set2018-07-12
K932436 — ECHOMARK INTRAUTERINE GUIDING CATHETER1995-11-16
K931476 — NOVY CORNUAL CANNULATION SET1995-07-28
K953314 — CONCEPTUS FALLOPIAN TUBE CATHETERIZATION SYSTEM1995-07-28

More clearances from Ovamed Corp.

view all

K951946 — HYSTEROSYS FLEXIBLE HYSTEROCOPE1995-11-20
K931167 — OVAMED FALLOPIAN OSTIAL ACCESS CATHETER1995-06-22
K943593 — SARATOGA MODULAR MINIATURE ENDOSCOPE SYSTEM1995-03-22
K931122 — OVAMED HSG CATHETER1995-01-30

Data sourced from openFDA. This site is unofficial and independent of the FDA.