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FDA 510(k)

GENERAL PATIENT MONITORS, MODELS: G3C/ G3D/ G3F/ G3G/ G3H

K-Number: K092970 · 2010-02-02

ApplicantGeneral Meditech, Inc.
Decision Date2010-02-02
Product CodeMHX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

GENERAL PATIENT MONITORS, MODELS: G3C/ G3D/ G3F/ G3G/ G3H is the device name listed in this FDA 510(k) record. The listed applicant is General Meditech, Inc.. It received FDA 510(k) clearance on 2010-02-02 under 510(k) number K092970. The device is classified under product code MHX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GENERAL PATIENT MONITORS, MODELS: G3C/ G3D/ G3F/ G3G/ G3H?

GENERAL PATIENT MONITORS, MODELS: G3C/ G3D/ G3F/ G3G/ G3H is a medical device that received FDA 510(k) clearance on 2010-02-02. The listed applicant is General Meditech, Inc.. The 510(k) number is K092970.

When did GENERAL PATIENT MONITORS, MODELS: G3C/ G3D/ G3F/ G3G/ G3H receive FDA 510(k) clearance?

GENERAL PATIENT MONITORS, MODELS: G3C/ G3D/ G3F/ G3G/ G3H received FDA 510(k) clearance on 2010-02-02, under 510(k) number K092970.

Who is the listed applicant for GENERAL PATIENT MONITORS, MODELS: G3C/ G3D/ G3F/ G3G/ G3H?

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

What is the FDA product code for GENERAL PATIENT MONITORS, MODELS: G3C/ G3D/ G3F/ G3G/ G3H?

The FDA product code for GENERAL PATIENT MONITORS, MODELS: G3C/ G3D/ G3F/ G3G/ G3H is MHX.

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 General Meditech, 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.

K082789G1B PULSE OXIMETER

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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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