ARTICULATED, LAPAROSCOPIC, AND SIDE-VIEWING T-PROBES— 510(k) K935157

Name: FDA 510(k) clearance K935157
Creator: U.S. Food and Drug Administration
Published: 1994-08-09

Substantially Equivalent

Regulatory Consultants TO the Medical Device Indus

FDA 510(k) clearance K935157 for ARTICULATED, LAPAROSCOPIC, AND SIDE-VIEWING T-PROBES, Substantially Equivalent on 1994-08-09. Applicant: Regulatory Consultants TO the Medical Device Indus. Device class: 2.

Clearance details

Applicant: Regulatory Consultants TO the Medical Device Indus
Product code: Code KPX
Device class: Class 2
Regulation: 21 CFR 892.1860
Advisory panel: Radiology
Date received: 1993-10-28
Decision date: 1994-08-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Sandy, UT, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KPX

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K945635 — TRANS X-10001995-02-01
K934850 — NUCLEAR ASSOCIATES PERSONNEL PROTECTIVE SHIELDS1993-11-22
K933035 — BCM-600TX1993-10-08
K925598 — BUCKYMATIC AUTOMATIC CHEST FILM CHANGER1993-02-01
K924423 — MWX-7440 HIGH SPEED BUCKY1993-01-15

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