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FDA 510(k)

ARI STANDARD ANESTHESIA RECORD

K-Number: K854213 · 1985-12-19

ApplicantAgilent Technologies, Inc.
Decision Date1985-12-19
Product CodeBSZ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

ARI STANDARD ANESTHESIA RECORD is the device name listed in this FDA 510(k) record. The listed applicant is Agilent Technologies, Inc.. It received FDA 510(k) clearance on 1985-12-19 under 510(k) number K854213. The device is classified under product code BSZ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARI STANDARD ANESTHESIA RECORD?

ARI STANDARD ANESTHESIA RECORD is a medical device that received FDA 510(k) clearance on 1985-12-19. The listed applicant is Agilent Technologies, Inc.. The 510(k) number is K854213.

When did ARI STANDARD ANESTHESIA RECORD receive FDA 510(k) clearance?

ARI STANDARD ANESTHESIA RECORD received FDA 510(k) clearance on 1985-12-19, under 510(k) number K854213.

Who is the listed applicant for ARI STANDARD ANESTHESIA RECORD?

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

What is the FDA product code for ARI STANDARD ANESTHESIA RECORD?

The FDA product code for ARI STANDARD ANESTHESIA RECORD is BSZ.

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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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