FDA 510(k)

CORNING TRANSPHOR

K-Number: K800544 · 1980-03-20

Decision Date1980-03-20

Product CodeJHX

Advisory CommitteeCH

DecisionSubstantially Equivalent

Device Summary

CORNING TRANSPHOR is the device name listed in this FDA 510(k) record. The listed applicant is Corning Medical & Scientific. It received FDA 510(k) clearance on 1980-03-20 under 510(k) number K800544. The device is classified under product code JHX. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CORNING TRANSPHOR?

CORNING TRANSPHOR is a medical device that received FDA 510(k) clearance on 1980-03-20. The listed applicant is Corning Medical & Scientific. The 510(k) number is K800544.

When did CORNING TRANSPHOR receive FDA 510(k) clearance?

CORNING TRANSPHOR received FDA 510(k) clearance on 1980-03-20, under 510(k) number K800544.

Who is the listed applicant for CORNING TRANSPHOR?

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

What is the FDA product code for CORNING TRANSPHOR?

The FDA product code for CORNING TRANSPHOR is JHX.

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_RECRUITING NCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITING NCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDED NCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Corning Medical & Scientific as applicant

K875122DISPOSABLE STERILE SYRINGE FILTERS K872273CORNING EASY WASH ELISA PLATES K872076CORNING DISPOSABLE ROLLER BOTTLES K863789CORNING ELISA PLATES K854024CORNING MAGIC MAB HCG RADIOIMMUNOASSAY K853634CORNING CELL WELLS-MULTIPLE WELL PLATES

View all 111 devices →

Related Devices (Code: JHX)

K234005Access CK-MBBeckman Coulter, Inc.K212648VITROS Immunodiagnostic Products CK-MB Reagent PackOrtho Clinical Diagnostics K163462AQT90 FLEX Myo Test Kit, AQT90 FLEX CKMB Test Kit, AQT90 FLEXRadiometer Medical Aps K120326AQT90 FLEX CKMB TEST KIT, AQT90 FLEX LQC MULTI-CHECK, LEVELS 1-3, AQT90 FLEX CKMB CAL CARTRIDGERadiometer Medical Aps K081360PATHFAST CK-MB-II, PATHFAST MYO-IIMitsubishi Kagaku Iatron K051650STRATUS CS ACUTE CARE MB ISOENZYME OF CREATINE KINASE (CKMB) TEST PAK; STRATUS CS ACUTE CARE CKMB TESTPAK.Dade Behring, 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.