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FDA 510(k)

CEDIA DAU CONTROLS

K-Number: K934650 · 1994-04-26

Decision Date1994-04-26
Product CodeDIF
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

CEDIA DAU CONTROLS is the device name listed in this FDA 510(k) record. The listed applicant is Medical Analysis Systems, Inc.. It received FDA 510(k) clearance on 1994-04-26 under 510(k) number K934650. The device is classified under product code DIF. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CEDIA DAU CONTROLS?

CEDIA DAU CONTROLS is a medical device that received FDA 510(k) clearance on 1994-04-26. The listed applicant is Medical Analysis Systems, Inc.. The 510(k) number is K934650.

When did CEDIA DAU CONTROLS receive FDA 510(k) clearance?

CEDIA DAU CONTROLS received FDA 510(k) clearance on 1994-04-26, under 510(k) number K934650.

Who is the listed applicant for CEDIA DAU CONTROLS?

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

What is the FDA product code for CEDIA DAU CONTROLS?

The FDA product code for CEDIA DAU CONTROLS is DIF.

Related Clinical Trials

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.

Other records listing Medical Analysis Systems, Inc. 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.

View all 107 devices →

Related Devices (Code: DIF)

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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