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FDA 510(k)

MODIFICATION ELECTRONIC CLINICAL THERMO-

K-Number: K830819 · 1983-04-06

Decision Date1983-04-06
Product CodeFLL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MODIFICATION ELECTRONIC CLINICAL THERMO- is the device name listed in this FDA 510(k) record. The listed applicant is Mon-A-Therm, Inc.. It received FDA 510(k) clearance on 1983-04-06 under 510(k) number K830819. The device is classified under product code FLL. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODIFICATION ELECTRONIC CLINICAL THERMO-?

MODIFICATION ELECTRONIC CLINICAL THERMO- is a medical device that received FDA 510(k) clearance on 1983-04-06. The listed applicant is Mon-A-Therm, Inc.. The 510(k) number is K830819.

When did MODIFICATION ELECTRONIC CLINICAL THERMO- receive FDA 510(k) clearance?

MODIFICATION ELECTRONIC CLINICAL THERMO- received FDA 510(k) clearance on 1983-04-06, under 510(k) number K830819.

Who is the listed applicant for MODIFICATION ELECTRONIC CLINICAL THERMO-?

The FDA 510(k) record lists Mon-A-Therm, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MODIFICATION ELECTRONIC CLINICAL THERMO-?

The FDA product code for MODIFICATION ELECTRONIC CLINICAL THERMO- is FLL.

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 Mon-A-Therm, 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.

View all 17 devices →

Related Devices (Code: FLL)

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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