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FDA 510(k)

SC/TEMP 300

K-Number: K810332 · 1981-05-18

ApplicantThought Technology , Ltd.
Decision Date1981-05-18
Product CodeHCC
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

SC/TEMP 300 is the device name listed in this FDA 510(k) record. The listed applicant is Thought Technology , Ltd.. It received FDA 510(k) clearance on 1981-05-18 under 510(k) number K810332. The device is classified under product code HCC. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SC/TEMP 300?

SC/TEMP 300 is a medical device that received FDA 510(k) clearance on 1981-05-18. The listed applicant is Thought Technology , Ltd.. The 510(k) number is K810332.

When did SC/TEMP 300 receive FDA 510(k) clearance?

SC/TEMP 300 received FDA 510(k) clearance on 1981-05-18, under 510(k) number K810332.

Who is the listed applicant for SC/TEMP 300?

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

What is the FDA product code for SC/TEMP 300?

The FDA product code for SC/TEMP 300 is HCC.

Other records listing Thought Technology , Ltd. as applicant

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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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