FUJI CR IMAGING PLATE— 510(k) K862414

Substantially Equivalent

Parexel Intl. Corp.

FDA 510(k) clearance K862414 for FUJI CR IMAGING PLATE, Substantially Equivalent on 1987-02-26. Applicant: Parexel Intl. Corp.. Device class: 1.

Clearance details

Applicant: Parexel Intl. Corp.
Product code: Code EAM
Device class: Class 1
Regulation: 21 CFR 892.1960
Advisory panel: Radiology
Date received: 1986-06-25
Decision date: 1987-02-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Cambridge, MA, US

Download summary PDF View on FDA.gov ↗

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More clearances from Parexel Intl. Corp.

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K904902 — SMA 26 TRANSDUCER1991-03-26
K884800 — ACTA GENOS ELECTROCARDIOGRAPH1989-06-22
K864519 — PHILIPS COMPUTED RADIOGRAPHY SYSTEM (PCR)1987-02-13

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