PAPILLION PROCTOSCOPE— 510(k) K914784

Substantially Equivalent

Oldelft Corp. of America

FDA 510(k) clearance K914784 for PAPILLION PROCTOSCOPE, Substantially Equivalent on 1992-06-05. Applicant: Oldelft Corp. of America. Device class: 2.

Clearance details

Applicant: Oldelft Corp. of America
Product code: Code KQA
Device class: Class 2
Regulation: 21 CFR 892.5900
Advisory panel: Radiology
Date received: 1991-10-23
Decision date: 1992-06-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Fairfax, VA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KQA

K885126 — PHILIPS RT250 COLLIMATOR (PK8050)1989-06-01
K844180 — THE MCP-70-SE SYSTEM1985-02-01
K790168 — COLLIMATOR, BILATERIAL1979-02-15

More clearances from Oldelft Corp. of America

K980296 — OLDELFT DIGIDELCA1998-04-17
K973219 — AMBER DU1997-10-08
K946128 — SIMULIX-HP1995-05-12
K950037 — N 800 HF1995-02-15
K932848 — SIMULIX-MC CT EXTENSION1994-03-22

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