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FDA 510(k)

MEMCO 300 FILM CHANGER

K-Number: K792068 · 1979-11-16

ApplicantMemco, Inc.
Decision Date1979-11-16
Product CodeKPX
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MEMCO 300 FILM CHANGER is the device name listed in this FDA 510(k) record. The listed applicant is Memco, Inc.. It received FDA 510(k) clearance on 1979-11-16 under 510(k) number K792068. The device is classified under product code KPX. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEMCO 300 FILM CHANGER?

MEMCO 300 FILM CHANGER is a medical device that received FDA 510(k) clearance on 1979-11-16. The listed applicant is Memco, Inc.. The 510(k) number is K792068.

When did MEMCO 300 FILM CHANGER receive FDA 510(k) clearance?

MEMCO 300 FILM CHANGER received FDA 510(k) clearance on 1979-11-16, under 510(k) number K792068.

Who is the listed applicant for MEMCO 300 FILM CHANGER?

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

What is the FDA product code for MEMCO 300 FILM CHANGER?

The FDA product code for MEMCO 300 FILM CHANGER is KPX.

Related Clinical Trials

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.

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Related Devices (Code: KPX)

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.

K945635TRANS X-1000Canon USA, Inc.K935157ARTICULATED, LAPAROSCOPIC, AND SIDE-VIEWING T-PROBESRegulatory Consultants TO the Medical Device IndusK934850NUCLEAR ASSOCIATES PERSONNEL PROTECTIVE SHIELDSVictoreen, Inc.K933035BCM-600TXB C Medical , Ltd.K925598BUCKYMATIC AUTOMATIC CHEST FILM CHANGERAcoma Medical Imaging, Inc.K924423MWX-7440 HIGH SPEED BUCKYMidwest X-Ray Equipment Co.

Official Source

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

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