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FDA 510(k)

ANESTHESIA BREATHING CIRCUITS

K-Number: K830470 · 1983-03-24

Decision Date1983-03-24
Product CodeCAI
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

ANESTHESIA BREATHING CIRCUITS is the device name listed in this FDA 510(k) record. The listed applicant is Mon-A-Therm, Inc.. It received FDA 510(k) clearance on 1983-03-24 under 510(k) number K830470. The device is classified under product code CAI. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANESTHESIA BREATHING CIRCUITS?

ANESTHESIA BREATHING CIRCUITS is a medical device that received FDA 510(k) clearance on 1983-03-24. The listed applicant is Mon-A-Therm, Inc.. The 510(k) number is K830470.

When did ANESTHESIA BREATHING CIRCUITS receive FDA 510(k) clearance?

ANESTHESIA BREATHING CIRCUITS received FDA 510(k) clearance on 1983-03-24, under 510(k) number K830470.

Who is the listed applicant for ANESTHESIA BREATHING CIRCUITS?

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

What is the FDA product code for ANESTHESIA BREATHING CIRCUITS?

The FDA product code for ANESTHESIA BREATHING CIRCUITS is CAI.

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 Mon-A-Therm, 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 17 devices →

Related Devices (Code: CAI)

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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