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FDA 510(k)

MODEL A300CL CLINICAL REFRACTOMETER

K-Number: K941904 · 1994-12-13

ApplicantVee Gee Scientific, Inc.
Decision Date1994-12-13
Product CodeJRE
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

MODEL A300CL CLINICAL REFRACTOMETER is the device name listed in this FDA 510(k) record. The listed applicant is Vee Gee Scientific, Inc.. It received FDA 510(k) clearance on 1994-12-13 under 510(k) number K941904. The device is classified under product code JRE. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL A300CL CLINICAL REFRACTOMETER?

MODEL A300CL CLINICAL REFRACTOMETER is a medical device that received FDA 510(k) clearance on 1994-12-13. The listed applicant is Vee Gee Scientific, Inc.. The 510(k) number is K941904.

When did MODEL A300CL CLINICAL REFRACTOMETER receive FDA 510(k) clearance?

MODEL A300CL CLINICAL REFRACTOMETER received FDA 510(k) clearance on 1994-12-13, under 510(k) number K941904.

Who is the listed applicant for MODEL A300CL CLINICAL REFRACTOMETER?

The FDA 510(k) record lists Vee Gee Scientific, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MODEL A300CL CLINICAL REFRACTOMETER?

The FDA product code for MODEL A300CL CLINICAL REFRACTOMETER is JRE.

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 Vee Gee Scientific, Inc. 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.

K941906MODEL 2730 CLINICAL REFRACTOMETERK941901MODEL 2721 CLINICAL REFRACTOMETERK941903MODEL 2740 CLINICAL REFRACTOMETERK941905MODEL 3461 CLINICAL REFRACTOMETERK941902MODEL 3471 CLINICAL REFRACTOMETER

Related Devices (Code: JRE)

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.

K954977URINE REAGENTS STRIPS-8 PARAMETERS (MODIFICATION)Teco DiagnosticsK941906MODEL 2730 CLINICAL REFRACTOMETERVee Gee Scientific, Inc.K941903MODEL 2740 CLINICAL REFRACTOMETERVee Gee Scientific, Inc.K941901MODEL 2721 CLINICAL REFRACTOMETERVee Gee Scientific, Inc.K941905MODEL 3461 CLINICAL REFRACTOMETERVee Gee Scientific, Inc.K941902MODEL 3471 CLINICAL REFRACTOMETERVee Gee Scientific, 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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