PEDIATRIC ANESTHESIA CIRCUIT
K-Number: K801111 · 1980-05-23
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Device Summary
Frequently Asked Questions
What is the PEDIATRIC ANESTHESIA CIRCUIT?
PEDIATRIC ANESTHESIA CIRCUIT is a medical device that received FDA 510(k) clearance on 1980-05-23. The listed applicant is Vital Signs, Inc.. The 510(k) number is K801111.
When did PEDIATRIC ANESTHESIA CIRCUIT receive FDA 510(k) clearance?
PEDIATRIC ANESTHESIA CIRCUIT received FDA 510(k) clearance on 1980-05-23, under 510(k) number K801111.
Who is the listed applicant for PEDIATRIC ANESTHESIA CIRCUIT?
The FDA 510(k) record lists Vital Signs, Inc. 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 Vital Signs, 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: 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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