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FDA 510(k)

HOT PROBE MODEL 6001

K-Number: K832179 · 1983-10-04

ApplicantAnalytic Technology
Decision Date1983-10-04
Product CodeEEG
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

HOT PROBE MODEL 6001 is the device name listed in this FDA 510(k) record. The listed applicant is Analytic Technology. It received FDA 510(k) clearance on 1983-10-04 under 510(k) number K832179. The device is classified under product code EEG. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HOT PROBE MODEL 6001?

HOT PROBE MODEL 6001 is a medical device that received FDA 510(k) clearance on 1983-10-04. The listed applicant is Analytic Technology. The 510(k) number is K832179.

When did HOT PROBE MODEL 6001 receive FDA 510(k) clearance?

HOT PROBE MODEL 6001 received FDA 510(k) clearance on 1983-10-04, under 510(k) number K832179.

Who is the listed applicant for HOT PROBE MODEL 6001?

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

What is the FDA product code for HOT PROBE MODEL 6001?

The FDA product code for HOT PROBE MODEL 6001 is EEG.

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Other records listing Analytic Technology as applicant

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Related Devices (Code: EEG)

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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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