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FDA 510(k)

RIA KIT, PROSTATIC ACID

K-Number: K790580 · 1979-05-25

ApplicantMonitor Science Corp.
Decision Date1979-05-25
Product CodeJFH
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

RIA KIT, PROSTATIC ACID is the device name listed in this FDA 510(k) record. The listed applicant is Monitor Science Corp.. It received FDA 510(k) clearance on 1979-05-25 under 510(k) number K790580. The device is classified under product code JFH. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RIA KIT, PROSTATIC ACID?

RIA KIT, PROSTATIC ACID is a medical device that received FDA 510(k) clearance on 1979-05-25. The listed applicant is Monitor Science Corp.. The 510(k) number is K790580.

When did RIA KIT, PROSTATIC ACID receive FDA 510(k) clearance?

RIA KIT, PROSTATIC ACID received FDA 510(k) clearance on 1979-05-25, under 510(k) number K790580.

Who is the listed applicant for RIA KIT, PROSTATIC ACID?

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

What is the FDA product code for RIA KIT, PROSTATIC ACID?

The FDA product code for RIA KIT, PROSTATIC ACID is JFH.

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 Monitor Science 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.

K780949BIO-MONITOR AMIKACINK780950BIO-MONITOR TOBRAMYCINK780951BIO-MONITOR GENTAMICINK772038KANAMYCIN RIAK772039BETA-HCG RIA

Related Devices (Code: JFH)

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.

K000257IMMULITE 2000 PAP, MODELS L2KPA2, L2KPA6Diagnostic Products Corp.K981573UBI MAGIWEL PAP (PROSTATIC ACID PHOSPHATASE) EIA QUANTITATVEUnited Biotech, Inc.K964756PROSTATIC ACID PHOSPHATASE REAGENT TEST/PROSTATIC ACID PHOSPHATASE REAGENT KITWano-Tech Corp.K931701IMMULITE PAPDiagnostic Products Corp.K925377IMX PAPAbbott LaboratoriesK921745HYBRITECH STRATUS PAP FLUOROMETRIC ENZYME IMMUNOHybritech, 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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