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FDA 510(k)

PEDIATRIC ANESTHESIA CIRCUITS

K-Number: K932192 · 1993-07-02

Decision Date1993-07-02
Product CodeCAI
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

PEDIATRIC ANESTHESIA CIRCUITS is the device name listed in this FDA 510(k) record. The listed applicant is Life Shield Healthcare Products, Inc.. It received FDA 510(k) clearance on 1993-07-02 under 510(k) number K932192. 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 ANESTHESIA CIRCUITS?

PEDIATRIC ANESTHESIA CIRCUITS is a medical device that received FDA 510(k) clearance on 1993-07-02. The listed applicant is Life Shield Healthcare Products, Inc.. The 510(k) number is K932192.

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

PEDIATRIC ANESTHESIA CIRCUITS received FDA 510(k) clearance on 1993-07-02, under 510(k) number K932192.

Who is the listed applicant for PEDIATRIC ANESTHESIA CIRCUITS?

The FDA 510(k) record lists Life Shield Healthcare Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PEDIATRIC ANESTHESIA CIRCUITS?

The FDA product code for PEDIATRIC ANESTHESIA 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 Life Shield Healthcare Products, 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 17 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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