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FDA 510(k)

NASAL INTERFACE MODEL 7910

K-Number: K974453 · 1998-08-04

Decision Date1998-08-04
Product CodeBZD
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

NASAL INTERFACE MODEL 7910 is the device name listed in this FDA 510(k) record. The listed applicant is Healthdyne Technologies, Inc.. It received FDA 510(k) clearance on 1998-08-04 under 510(k) number K974453. The device is classified under product code BZD. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NASAL INTERFACE MODEL 7910?

NASAL INTERFACE MODEL 7910 is a medical device that received FDA 510(k) clearance on 1998-08-04. The listed applicant is Healthdyne Technologies, Inc.. The 510(k) number is K974453.

When did NASAL INTERFACE MODEL 7910 receive FDA 510(k) clearance?

NASAL INTERFACE MODEL 7910 received FDA 510(k) clearance on 1998-08-04, under 510(k) number K974453.

Who is the listed applicant for NASAL INTERFACE MODEL 7910?

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

What is the FDA product code for NASAL INTERFACE MODEL 7910?

The FDA product code for NASAL INTERFACE MODEL 7910 is BZD.

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 Healthdyne 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 9 devices →

Related Devices (Code: BZD)

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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