INTRAUTERINE CATHETER— 510(k) K861305

Substantially Equivalent

Ram Development

FDA 510(k) clearance K861305 for INTRAUTERINE CATHETER, Substantially Equivalent on 1986-12-11. Applicant: Ram Development. Device class: 2.

Clearance details

Applicant: Ram Development
Product code: Code HDR
Device class: Class 2
Regulation: 21 CFR 884.5250
Advisory panel: Obstetrics/Gynecology
Date received: 1986-04-07
Decision date: 1986-12-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Israel, IL

Download summary PDF View on FDA.gov ↗

Recent devices under product code HDR

K242031 — Béa Applicator (BAP-GB-01)2025-04-02
K222969 — FERTI-LILY Conception Cup2023-06-23
K993953 — OVES CERVICAL CAP2000-03-21
K945131 — IMAGYN INTRAUTERINE INSEMINATION DEVICE1995-05-15
K950714 — COOK INSEMINATION CUP1995-05-11

More clearances from Ram Development

K862691 — STOPCOCK1986-07-28

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