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FDA 510(k)

CENTURION-II, MODEL 3103 APNEA/BRADY CARDIA TRACHY

K-Number: K851889 · 1985-10-23

ApplicantClinical Data, Inc.
Decision Date1985-10-23
Product CodeBZQ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

CENTURION-II, MODEL 3103 APNEA/BRADY CARDIA TRACHY is the device name listed in this FDA 510(k) record. The listed applicant is Clinical Data, Inc.. It received FDA 510(k) clearance on 1985-10-23 under 510(k) number K851889. The device is classified under product code BZQ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CENTURION-II, MODEL 3103 APNEA/BRADY CARDIA TRACHY?

CENTURION-II, MODEL 3103 APNEA/BRADY CARDIA TRACHY is a medical device that received FDA 510(k) clearance on 1985-10-23. The listed applicant is Clinical Data, Inc.. The 510(k) number is K851889.

When did CENTURION-II, MODEL 3103 APNEA/BRADY CARDIA TRACHY receive FDA 510(k) clearance?

CENTURION-II, MODEL 3103 APNEA/BRADY CARDIA TRACHY received FDA 510(k) clearance on 1985-10-23, under 510(k) number K851889.

Who is the listed applicant for CENTURION-II, MODEL 3103 APNEA/BRADY CARDIA TRACHY?

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

What is the FDA product code for CENTURION-II, MODEL 3103 APNEA/BRADY CARDIA TRACHY?

The FDA product code for CENTURION-II, MODEL 3103 APNEA/BRADY CARDIA TRACHY is BZQ.

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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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