Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

OXFORD OPTRONIX MPM 3S

K-Number: K914397 · 1992-11-16

ApplicantDia-Stron, Ltd.
Decision Date1992-11-16
Product CodeFTI
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

OXFORD OPTRONIX MPM 3S is the device name listed in this FDA 510(k) record. The listed applicant is Dia-Stron, Ltd.. It received FDA 510(k) clearance on 1992-11-16 under 510(k) number K914397. The device is classified under product code FTI. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OXFORD OPTRONIX MPM 3S?

OXFORD OPTRONIX MPM 3S is a medical device that received FDA 510(k) clearance on 1992-11-16. The listed applicant is Dia-Stron, Ltd.. The 510(k) number is K914397.

When did OXFORD OPTRONIX MPM 3S receive FDA 510(k) clearance?

OXFORD OPTRONIX MPM 3S received FDA 510(k) clearance on 1992-11-16, under 510(k) number K914397.

Who is the listed applicant for OXFORD OPTRONIX MPM 3S?

The FDA 510(k) record lists Dia-Stron, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for OXFORD OPTRONIX MPM 3S?

The FDA product code for OXFORD OPTRONIX MPM 3S is FTI.

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

Related Devices (Code: FTI)

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.

K971455CLARUS MODEL 5197 SIGHTLITEClarus Medical Systems, 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.

↑