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FDA 510(k)

LIEBEL-FLARSHEIM AFC 1000 X-RAY FILM

K-Number: K841732 · 1984-06-05

ApplicantSybron Corp.
Decision Date1984-06-05
Product CodeIZP
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

LIEBEL-FLARSHEIM AFC 1000 X-RAY FILM is the device name listed in this FDA 510(k) record. The listed applicant is Sybron Corp.. It received FDA 510(k) clearance on 1984-06-05 under 510(k) number K841732. The device is classified under product code IZP. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIEBEL-FLARSHEIM AFC 1000 X-RAY FILM?

LIEBEL-FLARSHEIM AFC 1000 X-RAY FILM is a medical device that received FDA 510(k) clearance on 1984-06-05. The listed applicant is Sybron Corp.. The 510(k) number is K841732.

When did LIEBEL-FLARSHEIM AFC 1000 X-RAY FILM receive FDA 510(k) clearance?

LIEBEL-FLARSHEIM AFC 1000 X-RAY FILM received FDA 510(k) clearance on 1984-06-05, under 510(k) number K841732.

Who is the listed applicant for LIEBEL-FLARSHEIM AFC 1000 X-RAY FILM?

The FDA 510(k) record lists Sybron Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LIEBEL-FLARSHEIM AFC 1000 X-RAY FILM?

The FDA product code for LIEBEL-FLARSHEIM AFC 1000 X-RAY FILM is IZP.

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Other records listing Sybron Corp. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K862284SEALITEK854855PROOF ALGINATE IMPRESSION MATERIALK844092DIAGNOSTIC MICROSOPCE SLIDESK842132TYCOS SELF-CHECK/DIGITAL FEVER THERMOK841910KERR SEALAPEX ROOT CANAL SEALERK840407KERR RESIN BONDED BRIDGE CEMENT

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Related Devices (Code: IZP)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K934944MPQ-42Elema-Schonander, Inc.K911888PHILIPS ANGIOPROPhilips Medical Systems North America, Inc.K904144PULMOVISION CHEST RADIOGRAPHY X-RAY SYSTEMMallinckrodt Group, Inc.K904103SEP 90Elema-Schonander, Inc.K874451OMNIPLANE 200 FILM CHANGER SYSTEMMedrad, Inc.K854251THE CSE FILM CHANGER SYSTEMChanger Service & Engineering, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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