Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

CO2 GAS WARMER II, MODEL 6-800-00

K-Number: K992381 · 1999-09-17

Decision Date1999-09-17
Product CodeHIF
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

CO2 GAS WARMER II, MODEL 6-800-00 is the device name listed in this FDA 510(k) record. The listed applicant is Northgate Technologies, Inc.. It received FDA 510(k) clearance on 1999-09-17 under 510(k) number K992381. The device is classified under product code HIF. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CO2 GAS WARMER II, MODEL 6-800-00?

CO2 GAS WARMER II, MODEL 6-800-00 is a medical device that received FDA 510(k) clearance on 1999-09-17. The listed applicant is Northgate Technologies, Inc.. The 510(k) number is K992381.

When did CO2 GAS WARMER II, MODEL 6-800-00 receive FDA 510(k) clearance?

CO2 GAS WARMER II, MODEL 6-800-00 received FDA 510(k) clearance on 1999-09-17, under 510(k) number K992381.

Who is the listed applicant for CO2 GAS WARMER II, MODEL 6-800-00?

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

What is the FDA product code for CO2 GAS WARMER II, MODEL 6-800-00?

The FDA product code for CO2 GAS WARMER II, MODEL 6-800-00 is HIF.

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 Northgate Technologies, 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 55 devices →

Related Devices (Code: HIF)

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.

↑