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FDA 510(k)

ULTRANET-S COLLIMATOR

K-Number: K894142 · 1989-11-06

ApplicantGE Medical Systems
Decision Date1989-11-06
Product CodeIZW
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ULTRANET-S COLLIMATOR is the device name listed in this FDA 510(k) record. The listed applicant is GE Medical Systems. It received FDA 510(k) clearance on 1989-11-06 under 510(k) number K894142. The device is classified under product code IZW. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ULTRANET-S COLLIMATOR?

ULTRANET-S COLLIMATOR is a medical device that received FDA 510(k) clearance on 1989-11-06. The listed applicant is GE Medical Systems. The 510(k) number is K894142.

When did ULTRANET-S COLLIMATOR receive FDA 510(k) clearance?

ULTRANET-S COLLIMATOR received FDA 510(k) clearance on 1989-11-06, under 510(k) number K894142.

Who is the listed applicant for ULTRANET-S COLLIMATOR?

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

What is the FDA product code for ULTRANET-S COLLIMATOR?

The FDA product code for ULTRANET-S COLLIMATOR is IZW.

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Other records listing GE Medical Systems as applicant

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Related Devices (Code: IZW)

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.

K101039SHIMADZU COLLIMATOR R-300Shimadzu Corp.K093572R650 QDASM COLLIMATOROmega Medical Imaging, Inc.K090578SHIMADZU COLLIMATOR R-30HShimadzu Corp.K091517RALCO, MODEL R225 ACSRalco S.R.L.K083029MODEL R605DASM AUTOMATIC X-RAY COLLIMATORRalco S.R.L.K072780MODEL R302DACS/A AUTOMATIC X-RAY COLLIMATORRalco S.R.L.

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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