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FDA 510(k)

BLAKE MEDICAL BREATHING TUBE SUPPORT

K-Number: K902604 · 1990-10-02

Decision Date1990-10-02
Product CodeCBH
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

BLAKE MEDICAL BREATHING TUBE SUPPORT is the device name listed in this FDA 510(k) record. The listed applicant is Blake Medical, Inc.. It received FDA 510(k) clearance on 1990-10-02 under 510(k) number K902604. The device is classified under product code CBH. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BLAKE MEDICAL BREATHING TUBE SUPPORT?

BLAKE MEDICAL BREATHING TUBE SUPPORT is a medical device that received FDA 510(k) clearance on 1990-10-02. The listed applicant is Blake Medical, Inc.. The 510(k) number is K902604.

When did BLAKE MEDICAL BREATHING TUBE SUPPORT receive FDA 510(k) clearance?

BLAKE MEDICAL BREATHING TUBE SUPPORT received FDA 510(k) clearance on 1990-10-02, under 510(k) number K902604.

Who is the listed applicant for BLAKE MEDICAL BREATHING TUBE SUPPORT?

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

What is the FDA product code for BLAKE MEDICAL BREATHING TUBE SUPPORT?

The FDA product code for BLAKE MEDICAL BREATHING TUBE SUPPORT is CBH.

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 Blake 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.

Related Devices (Code: CBH)

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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