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FDA 510(k)

HUMID-HEAT

K-Number: K993773 · 2000-09-13

ApplicantHudson Rcj AB
Decision Date2000-09-13
Product CodeBTT
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

HUMID-HEAT is the device name listed in this FDA 510(k) record. The listed applicant is Hudson Rcj AB. It received FDA 510(k) clearance on 2000-09-13 under 510(k) number K993773. The device is classified under product code BTT. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HUMID-HEAT?

HUMID-HEAT is a medical device that received FDA 510(k) clearance on 2000-09-13. The listed applicant is Hudson Rcj AB. The 510(k) number is K993773.

When did HUMID-HEAT receive FDA 510(k) clearance?

HUMID-HEAT received FDA 510(k) clearance on 2000-09-13, under 510(k) number K993773.

Who is the listed applicant for HUMID-HEAT?

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

What is the FDA product code for HUMID-HEAT?

The FDA product code for HUMID-HEAT is BTT.

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.

Related Devices (Code: BTT)

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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