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FDA 510(k)

GRAPHIC STRESS TELETHERMOMETRY

K-Number: K800491 · 1980-03-04

Decision Date1980-03-04
Product CodeIYM
Advisory CommitteeOB
DecisionUnknown

Device Summary

GRAPHIC STRESS TELETHERMOMETRY is the device name listed in this FDA 510(k) record. The listed applicant is Gst Laboratories of Ca, Inc.. It received FDA 510(k) clearance on 1980-03-04 under 510(k) number K800491. The device is classified under product code IYM. It was reviewed by the OB advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the GRAPHIC STRESS TELETHERMOMETRY?

GRAPHIC STRESS TELETHERMOMETRY is a medical device that received FDA 510(k) clearance on 1980-03-04. The listed applicant is Gst Laboratories of Ca, Inc.. The 510(k) number is K800491.

When did GRAPHIC STRESS TELETHERMOMETRY receive FDA 510(k) clearance?

GRAPHIC STRESS TELETHERMOMETRY received FDA 510(k) clearance on 1980-03-04, under 510(k) number K800491.

Who is the listed applicant for GRAPHIC STRESS TELETHERMOMETRY?

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

What is the FDA product code for GRAPHIC STRESS TELETHERMOMETRY?

The FDA product code for GRAPHIC STRESS TELETHERMOMETRY is IYM.

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.

Other records listing Gst Laboratories of Ca, 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.

Related Devices (Code: IYM)

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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