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FDA 510(k)

CONTROLLER, SERVO, INSPIRON

K-Number: K780630 · 1978-05-31

ApplicantC.R. Bard, Inc.
Decision Date1978-05-31
Product CodeBZE
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

CONTROLLER, SERVO, INSPIRON is the device name listed in this FDA 510(k) record. The listed applicant is C.R. Bard, Inc.. It received FDA 510(k) clearance on 1978-05-31 under 510(k) number K780630. The device is classified under product code BZE. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CONTROLLER, SERVO, INSPIRON?

CONTROLLER, SERVO, INSPIRON is a medical device that received FDA 510(k) clearance on 1978-05-31. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K780630.

When did CONTROLLER, SERVO, INSPIRON receive FDA 510(k) clearance?

CONTROLLER, SERVO, INSPIRON received FDA 510(k) clearance on 1978-05-31, under 510(k) number K780630.

Who is the listed applicant for CONTROLLER, SERVO, INSPIRON?

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

What is the FDA product code for CONTROLLER, SERVO, INSPIRON?

The FDA product code for CONTROLLER, SERVO, INSPIRON is BZE.

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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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