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FDA 510(k)

DISPOS. TYPE T THERMOCOUPLE TEMP.PROBE

K-Number: K830592 · 1983-05-18

Decision Date1983-05-18
Product CodeFLL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DISPOS. TYPE T THERMOCOUPLE TEMP.PROBE is the device name listed in this FDA 510(k) record. The listed applicant is Electromedics, Inc.. It received FDA 510(k) clearance on 1983-05-18 under 510(k) number K830592. 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 DISPOS. TYPE T THERMOCOUPLE TEMP.PROBE?

DISPOS. TYPE T THERMOCOUPLE TEMP.PROBE is a medical device that received FDA 510(k) clearance on 1983-05-18. The listed applicant is Electromedics, Inc.. The 510(k) number is K830592.

When did DISPOS. TYPE T THERMOCOUPLE TEMP.PROBE receive FDA 510(k) clearance?

DISPOS. TYPE T THERMOCOUPLE TEMP.PROBE received FDA 510(k) clearance on 1983-05-18, under 510(k) number K830592.

Who is the listed applicant for DISPOS. TYPE T THERMOCOUPLE TEMP.PROBE?

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

What is the FDA product code for DISPOS. TYPE T THERMOCOUPLE TEMP.PROBE?

The FDA product code for DISPOS. TYPE T THERMOCOUPLE TEMP.PROBE 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 Electromedics, 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 41 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

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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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