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FDA 510(k)

ACS PHENOBARBITAL

K-Number: K953021 · 1995-12-11

ApplicantCiba Corning Diagnostics Corp.
Decision Date1995-12-11
Product CodeDIS
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

ACS PHENOBARBITAL is the device name listed in this FDA 510(k) record. The listed applicant is Ciba Corning Diagnostics Corp.. It received FDA 510(k) clearance on 1995-12-11 under 510(k) number K953021. The device is classified under product code DIS. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACS PHENOBARBITAL?

ACS PHENOBARBITAL is a medical device that received FDA 510(k) clearance on 1995-12-11. The listed applicant is Ciba Corning Diagnostics Corp.. The 510(k) number is K953021.

When did ACS PHENOBARBITAL receive FDA 510(k) clearance?

ACS PHENOBARBITAL received FDA 510(k) clearance on 1995-12-11, under 510(k) number K953021.

Who is the listed applicant for ACS PHENOBARBITAL?

The FDA 510(k) record lists Ciba Corning Diagnostics Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ACS PHENOBARBITAL?

The FDA product code for ACS PHENOBARBITAL is DIS.

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Other records listing Ciba Corning Diagnostics Corp. as applicant

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.

K962559ACS CORTISOL IMMUNOASSAYK963251CIBA CORNING ACS;180 DPD ASSAYK961807CERTAIN HCT LEVEL A & LEVEL B/CVM HCT LEVELS 1,2,3, & 4K961657CIBA CORNING 400 SYSTEMK962021CIBA CORNING 348 SYSTEMK962126ACS CKMB II IMMUNOASSAY

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Related Devices (Code: DIS)

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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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