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FDA 510(k)

PEDIATRIC GAS SAMPLING CIRCUITS

K-Number: K932589 · 1993-07-22

Decision Date1993-07-22
Product CodeCAI
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

PEDIATRIC GAS SAMPLING CIRCUITS is the device name listed in this FDA 510(k) record. The listed applicant is Merit Medical Systems, Inc.. It received FDA 510(k) clearance on 1993-07-22 under 510(k) number K932589. The device is classified under product code CAI. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PEDIATRIC GAS SAMPLING CIRCUITS?

PEDIATRIC GAS SAMPLING CIRCUITS is a medical device that received FDA 510(k) clearance on 1993-07-22. The listed applicant is Merit Medical Systems, Inc.. The 510(k) number is K932589.

When did PEDIATRIC GAS SAMPLING CIRCUITS receive FDA 510(k) clearance?

PEDIATRIC GAS SAMPLING CIRCUITS received FDA 510(k) clearance on 1993-07-22, under 510(k) number K932589.

Who is the listed applicant for PEDIATRIC GAS SAMPLING CIRCUITS?

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

What is the FDA product code for PEDIATRIC GAS SAMPLING CIRCUITS?

The FDA product code for PEDIATRIC GAS SAMPLING CIRCUITS is CAI.

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 Merit Medical Systems, 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 159 devices →

Related Devices (Code: CAI)

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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