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FDA 510(k)

ANESTHASSIST

K-Number: K871564 · 1987-05-18

ApplicantAnestech, Inc.
Decision Date1987-05-18
Product CodeBRY
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

ANESTHASSIST is the device name listed in this FDA 510(k) record. The listed applicant is Anestech, Inc.. It received FDA 510(k) clearance on 1987-05-18 under 510(k) number K871564. The device is classified under product code BRY. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANESTHASSIST?

ANESTHASSIST is a medical device that received FDA 510(k) clearance on 1987-05-18. The listed applicant is Anestech, Inc.. The 510(k) number is K871564.

When did ANESTHASSIST receive FDA 510(k) clearance?

ANESTHASSIST received FDA 510(k) clearance on 1987-05-18, under 510(k) number K871564.

Who is the listed applicant for ANESTHASSIST?

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

What is the FDA product code for ANESTHASSIST?

The FDA product code for ANESTHASSIST is BRY.

Related Clinical Trials

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Related Devices (Code: BRY)

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.

K921710MOVIT DEVICEJohn J. Navar, M.D.K912346MEDIKEEPERMedikeeper, Inc.K901474ANESTHESIA WORKSTATIONSiemens Life Support SystemsK821307ANESTHECACHEMed-Life, Inc.

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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