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FDA 510(k)

INFANT CANNULA

K-Number: K873012 · 1988-05-02

Decision Date1988-05-02
Product CodeDQR
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

INFANT CANNULA is the device name listed in this FDA 510(k) record. The listed applicant is Gresco International, Inc.. It received FDA 510(k) clearance on 1988-05-02 under 510(k) number K873012. The device is classified under product code DQR. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INFANT CANNULA?

INFANT CANNULA is a medical device that received FDA 510(k) clearance on 1988-05-02. The listed applicant is Gresco International, Inc.. The 510(k) number is K873012.

When did INFANT CANNULA receive FDA 510(k) clearance?

INFANT CANNULA received FDA 510(k) clearance on 1988-05-02, under 510(k) number K873012.

Who is the listed applicant for INFANT CANNULA?

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

What is the FDA product code for INFANT CANNULA?

The FDA product code for INFANT CANNULA is DQR.

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.

Related Devices (Code: DQR)

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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