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FDA 510(k)

GLOVE-CHEK PORTABLE FLUID LEAKAGE SENSING DEVICE

K-Number: K913696 · 1992-02-18

ApplicantVertex Technical Group, Inc.
Decision Date1992-02-18
Product CodeLDQ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

GLOVE-CHEK PORTABLE FLUID LEAKAGE SENSING DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Vertex Technical Group, Inc.. It received FDA 510(k) clearance on 1992-02-18 under 510(k) number K913696. The device is classified under product code LDQ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GLOVE-CHEK PORTABLE FLUID LEAKAGE SENSING DEVICE?

GLOVE-CHEK PORTABLE FLUID LEAKAGE SENSING DEVICE is a medical device that received FDA 510(k) clearance on 1992-02-18. The listed applicant is Vertex Technical Group, Inc.. The 510(k) number is K913696.

When did GLOVE-CHEK PORTABLE FLUID LEAKAGE SENSING DEVICE receive FDA 510(k) clearance?

GLOVE-CHEK PORTABLE FLUID LEAKAGE SENSING DEVICE received FDA 510(k) clearance on 1992-02-18, under 510(k) number K913696.

Who is the listed applicant for GLOVE-CHEK PORTABLE FLUID LEAKAGE SENSING DEVICE?

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

What is the FDA product code for GLOVE-CHEK PORTABLE FLUID LEAKAGE SENSING DEVICE?

The FDA product code for GLOVE-CHEK PORTABLE FLUID LEAKAGE SENSING DEVICE is LDQ.

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Related Devices (Code: LDQ)

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.

K993797EC-7701 FLUID WARMING CABINETEnthermics Medical Systems, Inc.K992258HOT SHOT FLUID WARMER IV FLUIDSInfra-Med Technologies, Inc.K981032PIV SYSTEMMedical Solutions, Inc.K973747CONTROLLED TEMPERATURE CABINET SYSTEMSmithK955661ACU-HALTGlederer & Co., Inc.K955776ACU-LABGlederer & Co., 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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