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FDA 510(k)

COLLIMATOR, BILATERIAL

K-Number: K790168 · 1979-02-15

ApplicantCmsi
Decision Date1979-02-15
Product CodeKQA
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

COLLIMATOR, BILATERIAL is the device name listed in this FDA 510(k) record. The listed applicant is Cmsi. It received FDA 510(k) clearance on 1979-02-15 under 510(k) number K790168. The device is classified under product code KQA. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COLLIMATOR, BILATERIAL?

COLLIMATOR, BILATERIAL is a medical device that received FDA 510(k) clearance on 1979-02-15. The listed applicant is Cmsi. The 510(k) number is K790168.

When did COLLIMATOR, BILATERIAL receive FDA 510(k) clearance?

COLLIMATOR, BILATERIAL received FDA 510(k) clearance on 1979-02-15, under 510(k) number K790168.

Who is the listed applicant for COLLIMATOR, BILATERIAL?

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

What is the FDA product code for COLLIMATOR, BILATERIAL?

The FDA product code for COLLIMATOR, BILATERIAL is KQA.

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 Cmsi 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.

K893499CMS FAST CUT, CMS DIAMOND AND CMS WIRE PASSK790169TOMOGRAPHIC PROGRAMS

Related Devices (Code: KQA)

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.

K914784PAPILLION PROCTOSCOPEOldelft Corp. of AmericaK885126PHILIPS RT250 COLLIMATOR (PK8050)Perkins Mfg. Co.K844180THE MCP-70-SE SYSTEMEllis Pharmaceutical Consulting, Inc.

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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