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FDA 510(k)

4003 NON CONDUCTIVE ANESTHESIA CIRCUIT W/BREAT\GAS

K-Number: K851530 · 1985-04-25

Decision Date1985-04-25
Product CodeCAI
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

4003 NON CONDUCTIVE ANESTHESIA CIRCUIT W/BREAT\GAS is the device name listed in this FDA 510(k) record. The listed applicant is Sigma Medical, Inc.. It received FDA 510(k) clearance on 1985-04-25 under 510(k) number K851530. 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 4003 NON CONDUCTIVE ANESTHESIA CIRCUIT W/BREAT\GAS?

4003 NON CONDUCTIVE ANESTHESIA CIRCUIT W/BREAT\GAS is a medical device that received FDA 510(k) clearance on 1985-04-25. The listed applicant is Sigma Medical, Inc.. The 510(k) number is K851530.

When did 4003 NON CONDUCTIVE ANESTHESIA CIRCUIT W/BREAT\GAS receive FDA 510(k) clearance?

4003 NON CONDUCTIVE ANESTHESIA CIRCUIT W/BREAT\GAS received FDA 510(k) clearance on 1985-04-25, under 510(k) number K851530.

Who is the listed applicant for 4003 NON CONDUCTIVE ANESTHESIA CIRCUIT W/BREAT\GAS?

The FDA 510(k) record lists Sigma Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for 4003 NON CONDUCTIVE ANESTHESIA CIRCUIT W/BREAT\GAS?

The FDA product code for 4003 NON CONDUCTIVE ANESTHESIA CIRCUIT W/BREAT\GAS 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 Sigma Medical, 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 13 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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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