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FDA 510(k)

RINGCAPS

K-Number: K843362 · 1984-09-21

ApplicantMedical Technomics, Ltd.
Decision Date1984-09-21
Product CodeGIO
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

RINGCAPS is the device name listed in this FDA 510(k) record. The listed applicant is Medical Technomics, Ltd.. It received FDA 510(k) clearance on 1984-09-21 under 510(k) number K843362. The device is classified under product code GIO. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RINGCAPS?

RINGCAPS is a medical device that received FDA 510(k) clearance on 1984-09-21. The listed applicant is Medical Technomics, Ltd.. The 510(k) number is K843362.

When did RINGCAPS receive FDA 510(k) clearance?

RINGCAPS received FDA 510(k) clearance on 1984-09-21, under 510(k) number K843362.

Who is the listed applicant for RINGCAPS?

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

What is the FDA product code for RINGCAPS?

The FDA product code for RINGCAPS is GIO.

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.

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Other records listing Medical Technomics, Ltd. 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.

K844798EPPENDORF DILUTERK843608CAPILLARY BLOOD COLLECTION TUBEK843361MINICAPSK843607LABOPETTORK843606PRECISION DISPENSER

Related Devices (Code: GIO)

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.

K972969QUICK-DRAW CAPILLARY WHOLE BLOOD COLLECTION SYSTEMInnovative Medical Technologies, Inc.K941291MONOJECT SAMPLETTE SEPARATOR TUBESherwood Medical Co.K894851TRU-TRAXHumagen, Inc.K885324HEMA(PRO)TEC(TION)Medical Products Search, Inc.K885138CAPILLARY TUBE, BLOOD COLLECTIONCoeur Laboratories, Inc.K884623SAFE-TEC CAPILLARY BLOOD COLLECTION TUBESafe-Tec Clinical Products, 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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