VERIFLEX— 510(k) K854410

Substantially Equivalent

Old Delft Corp. of America

FDA 510(k) clearance K854410 for VERIFLEX, Substantially Equivalent on 1986-02-12. Applicant: Old Delft Corp. of America. Device class: 2.

Clearance details

Applicant: Old Delft Corp. of America
Product code: Code KPZ
Device class: Class 2
Regulation: 21 CFR 892.5900
Advisory panel: Radiology
Date received: 1985-11-01
Decision date: 1986-02-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Fairfax, VA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KPZ

K912249 — PATIENT DOSE MONITOR1991-08-30
K860469 — 37-701-1 PATIENT DOASE MONITOR WITH DETECTORS1986-04-16

More clearances from Old Delft Corp. of America

K862616 — AMBER-CHEST1986-09-02
K861431 — THERAPAX HT 150T1986-05-21

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