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FDA 510(k)

BCM-302 COLLIMATING CONE & COMPENSATIN

K-Number: K801949 · 1980-10-03

ApplicantB C Medical , Ltd.
Decision Date1980-10-03
Product CodeJZW
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

BCM-302 COLLIMATING CONE & COMPENSATIN 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 K801949. The device is classified under product code JZW. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BCM-302 COLLIMATING CONE & COMPENSATIN?

BCM-302 COLLIMATING CONE & COMPENSATIN 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 K801949.

When did BCM-302 COLLIMATING CONE & COMPENSATIN receive FDA 510(k) clearance?

BCM-302 COLLIMATING CONE & COMPENSATIN received FDA 510(k) clearance on 1980-10-03, under 510(k) number K801949.

Who is the listed applicant for BCM-302 COLLIMATING CONE & COMPENSATIN?

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-302 COLLIMATING CONE & COMPENSATIN?

The FDA product code for BCM-302 COLLIMATING CONE & COMPENSATIN is JZW.

Related Clinical Trials

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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: JZW)

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.

K001647BN PROSPEC SYSTEMDade Behring, Inc.K761234BEHRING LASER NEPHELOMETERBehring Diagnostics, Inc.K892223BEHRING NEPHELOMETER 100Behring Diagnostics, Inc.K873407RRT SYSTEM LASER REFLECTOMETER ANALYZERIncstar Corp.K873401TURBOXUnipath , Ltd.K801391DISC 120 TRANSPORTERTravenol Laboratories, S.A.

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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