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FDA 510(k)

KONICA QX-130APLUS AUTOMATIC X-RAY FILM PROCESSOR

K-Number: K931313 · 1993-09-07

ApplicantKonica Medical Corp.
Decision Date1993-09-07
Product CodeIXW
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

KONICA QX-130APLUS AUTOMATIC X-RAY FILM PROCESSOR is the device name listed in this FDA 510(k) record. The listed applicant is Konica Medical Corp.. It received FDA 510(k) clearance on 1993-09-07 under 510(k) number K931313. The device is classified under product code IXW. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KONICA QX-130APLUS AUTOMATIC X-RAY FILM PROCESSOR?

KONICA QX-130APLUS AUTOMATIC X-RAY FILM PROCESSOR is a medical device that received FDA 510(k) clearance on 1993-09-07. The listed applicant is Konica Medical Corp.. The 510(k) number is K931313.

When did KONICA QX-130APLUS AUTOMATIC X-RAY FILM PROCESSOR receive FDA 510(k) clearance?

KONICA QX-130APLUS AUTOMATIC X-RAY FILM PROCESSOR received FDA 510(k) clearance on 1993-09-07, under 510(k) number K931313.

Who is the listed applicant for KONICA QX-130APLUS AUTOMATIC X-RAY FILM PROCESSOR?

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

What is the FDA product code for KONICA QX-130APLUS AUTOMATIC X-RAY FILM PROCESSOR?

The FDA product code for KONICA QX-130APLUS AUTOMATIC X-RAY FILM PROCESSOR is IXW.

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Other records listing Konica Medical 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.

K990969KONICA SRX- 701 AUTOMATIC X-RAY FILM PROCESSORK963913MD100 & MM150K963914CM & CM DS-7K955583VIFSK931315KONICA SRX-501A AUTOMATIC X-RAY FILM PROCESSORK933830KONICA LD-4500 LASER DIGITIZER

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Related Devices (Code: IXW)

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.

K111167XTENDER FILM PROCESSOR, SPRINT FILM PROCESSOR MODEL XTENDER MODEL SPRINTVelopex International, Inc.K093503INTRAX FILM PROCESSORVelopex International, Inc.K091628OPTIMAX, COMPACT 2, OPTIMAX 2010, ECOMAXProtec GmbH & Co. KGK024342RADIOGRAPHIC FILM PROCESSOR, MODELS XP400 AND XP1000Daito Co., Ltd.K023801FILM PROCESSOR, MODEL LIFE RAY PRO 1000S.A.I.E.P. S.R.L.K023825FILM PROCESSOR, MODEL LIFE RAY PRO 2500S.A.I.E.P. S.R.L.

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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