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FDA 510(k)

NORTHGATE TECHNOLOGIES MODEL 7201 INSUFFLATOR

K-Number: K905481 · 1991-03-29

Decision Date1991-03-29
Product CodeHIF
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

NORTHGATE TECHNOLOGIES MODEL 7201 INSUFFLATOR 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 1991-03-29 under 510(k) number K905481. 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 NORTHGATE TECHNOLOGIES MODEL 7201 INSUFFLATOR?

NORTHGATE TECHNOLOGIES MODEL 7201 INSUFFLATOR is a medical device that received FDA 510(k) clearance on 1991-03-29. The listed applicant is Northgate Technologies, Inc.. The 510(k) number is K905481.

When did NORTHGATE TECHNOLOGIES MODEL 7201 INSUFFLATOR receive FDA 510(k) clearance?

NORTHGATE TECHNOLOGIES MODEL 7201 INSUFFLATOR received FDA 510(k) clearance on 1991-03-29, under 510(k) number K905481.

Who is the listed applicant for NORTHGATE TECHNOLOGIES MODEL 7201 INSUFFLATOR?

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 NORTHGATE TECHNOLOGIES MODEL 7201 INSUFFLATOR?

The FDA product code for NORTHGATE TECHNOLOGIES MODEL 7201 INSUFFLATOR 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

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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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