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FDA 510(k)

NOVOCHECK/CHECKPOINT/CONTROL SOLUTION

K-Number: K872049 · 1987-08-13

ApplicantGarid, Inc.
Decision Date1987-08-13
Product CodeCGA
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

NOVOCHECK/CHECKPOINT/CONTROL SOLUTION is the device name listed in this FDA 510(k) record. The listed applicant is Garid, Inc.. It received FDA 510(k) clearance on 1987-08-13 under 510(k) number K872049. The device is classified under product code CGA. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NOVOCHECK/CHECKPOINT/CONTROL SOLUTION?

NOVOCHECK/CHECKPOINT/CONTROL SOLUTION is a medical device that received FDA 510(k) clearance on 1987-08-13. The listed applicant is Garid, Inc.. The 510(k) number is K872049.

When did NOVOCHECK/CHECKPOINT/CONTROL SOLUTION receive FDA 510(k) clearance?

NOVOCHECK/CHECKPOINT/CONTROL SOLUTION received FDA 510(k) clearance on 1987-08-13, under 510(k) number K872049.

Who is the listed applicant for NOVOCHECK/CHECKPOINT/CONTROL SOLUTION?

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

What is the FDA product code for NOVOCHECK/CHECKPOINT/CONTROL SOLUTION?

The FDA product code for NOVOCHECK/CHECKPOINT/CONTROL SOLUTION is CGA.

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 Garid, 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.

K853733MED-PEN/MED-POINT

Related Devices (Code: CGA)

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.

K252488ABL90 FLEX PLUS SystemRadiometer Medicals ApsK210933YSI 2900C Biochemistry AnalyzerYsi, Inc.K220328EasyStat 300Medica CorporationK223179Cholestech LDX ™ SystemAlere San Diego, Inc.K223755i-STAT G cartridge with the i-STAT 1 SystemAbbott Point of Care, Inc.K223710i-STAT CG8+ cartridge with the i-STAT 1 SystemAbbott Point of Care, 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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