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FDA 510(k)

RINN UNIVERSAL COLLIMATOR

K-Number: K932134 · 1993-07-26

ApplicantRinn Corp.
Decision Date1993-07-26
Product CodeIZX
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

RINN UNIVERSAL COLLIMATOR is the device name listed in this FDA 510(k) record. The listed applicant is Rinn Corp.. It received FDA 510(k) clearance on 1993-07-26 under 510(k) number K932134. The device is classified under product code IZX. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RINN UNIVERSAL COLLIMATOR?

RINN UNIVERSAL COLLIMATOR is a medical device that received FDA 510(k) clearance on 1993-07-26. The listed applicant is Rinn Corp.. The 510(k) number is K932134.

When did RINN UNIVERSAL COLLIMATOR receive FDA 510(k) clearance?

RINN UNIVERSAL COLLIMATOR received FDA 510(k) clearance on 1993-07-26, under 510(k) number K932134.

Who is the listed applicant for RINN UNIVERSAL COLLIMATOR?

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

What is the FDA product code for RINN UNIVERSAL COLLIMATOR?

The FDA product code for RINN UNIVERSAL COLLIMATOR is IZX.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Rinn 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.

K913885RINN E-Z CAPPERK828605BEAM LIMITING DEVICEK813378UNI-BITE DENTAL X-RAY FILM HOLDERK772313X-RAY CO-ORDINATOR

Related Devices (Code: IZX)

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.

K110856RALCORalco S.R.L.K101036SHIMADZU COLLIMATOR R-20JShimadzu Corp.K042840SHIMADZU COLLIMATOR R-20JShimadzu Corp.K031771SHIMADZU COLLIMATOR R-30HShimadzu Corp.K981267FACTS MONOBLOCKDynarad Corp.K974240LIGHTLINE-MWuestec Medical, 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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