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FDA 510(k)

BCM-600 MINI-SIX EXTRA LG. FIELD ANGIO

K-Number: K801950 · 1980-10-03

ApplicantB C Medical , Ltd.
Decision Date1980-10-03
Product CodeKPX
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

BCM-600 MINI-SIX EXTRA LG. FIELD ANGIO is the device name listed in this FDA 510(k) record. The listed applicant is B C Medical , Ltd.. It received FDA 510(k) clearance on 1980-10-03 under 510(k) number K801950. 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 BCM-600 MINI-SIX EXTRA LG. FIELD ANGIO?

BCM-600 MINI-SIX EXTRA LG. FIELD ANGIO is a medical device that received FDA 510(k) clearance on 1980-10-03. The listed applicant is B C Medical , Ltd.. The 510(k) number is K801950.

When did BCM-600 MINI-SIX EXTRA LG. FIELD ANGIO receive FDA 510(k) clearance?

BCM-600 MINI-SIX EXTRA LG. FIELD ANGIO received FDA 510(k) clearance on 1980-10-03, under 510(k) number K801950.

Who is the listed applicant for BCM-600 MINI-SIX EXTRA LG. FIELD ANGIO?

The FDA 510(k) record lists B C Medical , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BCM-600 MINI-SIX EXTRA LG. FIELD ANGIO?

The FDA product code for BCM-600 MINI-SIX EXTRA LG. FIELD ANGIO 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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Other records listing B C Medical , Ltd. 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.

K946378BCM 400CPK933100ARC-600K933035BCM-600TXK920862BCM-400CK890306BCM-ARC 105 X-RAY MOBILE UNITK870205ROTAX-II BI-PLANE CIRCULAR ARM

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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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