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FDA 510(k)

WARMING LISTHTS #96H & 96HT

K-Number: K812745 · 1981-11-02

Decision Date1981-11-02
Product CodeFMT
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

WARMING LISTHTS #96H & 96HT is the device name listed in this FDA 510(k) record. The listed applicant is J. H. Emerson Co.. It received FDA 510(k) clearance on 1981-11-02 under 510(k) number K812745. The device is classified under product code FMT. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WARMING LISTHTS #96H & 96HT?

WARMING LISTHTS #96H & 96HT is a medical device that received FDA 510(k) clearance on 1981-11-02. The listed applicant is J. H. Emerson Co.. The 510(k) number is K812745.

When did WARMING LISTHTS #96H & 96HT receive FDA 510(k) clearance?

WARMING LISTHTS #96H & 96HT received FDA 510(k) clearance on 1981-11-02, under 510(k) number K812745.

Who is the listed applicant for WARMING LISTHTS #96H & 96HT?

The FDA 510(k) record lists J. H. Emerson Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for WARMING LISTHTS #96H & 96HT?

The FDA product code for WARMING LISTHTS #96H & 96HT is FMT.

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 J. H. Emerson Co. 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.

View all 25 devices →

Related Devices (Code: FMT)

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

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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