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FDA 510(k)

SPECTRUM AUTOMATIC CHEST UNIT MODEL C

K-Number: K791811 · 1979-10-26

ApplicantSpectrum X-Ray Corp.
Decision Date1979-10-26
Product CodeKPX
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SPECTRUM AUTOMATIC CHEST UNIT MODEL C is the device name listed in this FDA 510(k) record. The listed applicant is Spectrum X-Ray Corp.. It received FDA 510(k) clearance on 1979-10-26 under 510(k) number K791811. 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 SPECTRUM AUTOMATIC CHEST UNIT MODEL C?

SPECTRUM AUTOMATIC CHEST UNIT MODEL C is a medical device that received FDA 510(k) clearance on 1979-10-26. The listed applicant is Spectrum X-Ray Corp.. The 510(k) number is K791811.

When did SPECTRUM AUTOMATIC CHEST UNIT MODEL C receive FDA 510(k) clearance?

SPECTRUM AUTOMATIC CHEST UNIT MODEL C received FDA 510(k) clearance on 1979-10-26, under 510(k) number K791811.

Who is the listed applicant for SPECTRUM AUTOMATIC CHEST UNIT MODEL C?

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

What is the FDA product code for SPECTRUM AUTOMATIC CHEST UNIT MODEL C?

The FDA product code for SPECTRUM AUTOMATIC CHEST UNIT MODEL C is KPX.

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Other records listing Spectrum X-Ray 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.

K933134SPECTRUM DG-P7000 PEDIATRIC CRADLEK931563SPECTRUM MARK I SPECIAL PROCEDURES TABLEK870707PENTAMAX 1 MODEL B TABLE SYSTEMK840463DIGITAL CRADLEK834494SPECTRUM X-RAY CORPK827450SIMPLAMATIC III

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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

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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