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FDA 510(k)

HEAT MOISTURE CONDENSER

K-Number: K923910 · 1993-01-26

Decision Date1993-01-26
Product CodeBYD
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

HEAT MOISTURE CONDENSER is the device name listed in this FDA 510(k) record. The listed applicant is Concord/Portex. It received FDA 510(k) clearance on 1993-01-26 under 510(k) number K923910. The device is classified under product code BYD. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HEAT MOISTURE CONDENSER?

HEAT MOISTURE CONDENSER is a medical device that received FDA 510(k) clearance on 1993-01-26. The listed applicant is Concord/Portex. The 510(k) number is K923910.

When did HEAT MOISTURE CONDENSER receive FDA 510(k) clearance?

HEAT MOISTURE CONDENSER received FDA 510(k) clearance on 1993-01-26, under 510(k) number K923910.

Who is the listed applicant for HEAT MOISTURE CONDENSER?

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

What is the FDA product code for HEAT MOISTURE CONDENSER?

The FDA product code for HEAT MOISTURE CONDENSER is BYD.

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 Concord/Portex 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 23 devices →

Related Devices (Code: BYD)

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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