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FDA 510(k)

ANESTHESIOLOGY DEVICES

K-Number: K820046 · 1982-01-29

ApplicantBentley Laboratories, Inc.
Decision Date1982-01-29
Product CodeDRS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ANESTHESIOLOGY DEVICES is the device name listed in this FDA 510(k) record. The listed applicant is Bentley Laboratories, Inc.. It received FDA 510(k) clearance on 1982-01-29 under 510(k) number K820046. The device is classified under product code DRS. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANESTHESIOLOGY DEVICES?

ANESTHESIOLOGY DEVICES is a medical device that received FDA 510(k) clearance on 1982-01-29. The listed applicant is Bentley Laboratories, Inc.. The 510(k) number is K820046.

When did ANESTHESIOLOGY DEVICES receive FDA 510(k) clearance?

ANESTHESIOLOGY DEVICES received FDA 510(k) clearance on 1982-01-29, under 510(k) number K820046.

Who is the listed applicant for ANESTHESIOLOGY DEVICES?

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

What is the FDA product code for ANESTHESIOLOGY DEVICES?

The FDA product code for ANESTHESIOLOGY DEVICES is DRS.

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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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