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FDA 510(k)

PEDIATRIC ANESTHESIA CIRCUIT

K-Number: K770549 · 1977-03-30

Decision Date1977-03-30
Product CodeCAI
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

PEDIATRIC ANESTHESIA CIRCUIT is the device name listed in this FDA 510(k) record. The listed applicant is Inspiron Corp.. It received FDA 510(k) clearance on 1977-03-30 under 510(k) number K770549. 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 CIRCUIT?

PEDIATRIC ANESTHESIA CIRCUIT is a medical device that received FDA 510(k) clearance on 1977-03-30. The listed applicant is Inspiron Corp.. The 510(k) number is K770549.

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

PEDIATRIC ANESTHESIA CIRCUIT received FDA 510(k) clearance on 1977-03-30, under 510(k) number K770549.

Who is the listed applicant for PEDIATRIC ANESTHESIA CIRCUIT?

The FDA 510(k) record lists Inspiron Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PEDIATRIC ANESTHESIA CIRCUIT?

The FDA product code for PEDIATRIC ANESTHESIA CIRCUIT 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 Inspiron Corp. 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 20 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

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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