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FDA 510(k)

CADD CHECKVALVE ADMINISTRATION SET, MODEL 21-7090

K-Number: K000942 · 2000-04-27

Decision Date2000-04-27
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CADD CHECKVALVE ADMINISTRATION SET, MODEL 21-7090 is the device name listed in this FDA 510(k) record. The listed applicant is Sims Deltec, Inc.. It received FDA 510(k) clearance on 2000-04-27 under 510(k) number K000942. The device is classified under product code FPA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CADD CHECKVALVE ADMINISTRATION SET, MODEL 21-7090?

CADD CHECKVALVE ADMINISTRATION SET, MODEL 21-7090 is a medical device that received FDA 510(k) clearance on 2000-04-27. The listed applicant is Sims Deltec, Inc.. The 510(k) number is K000942.

When did CADD CHECKVALVE ADMINISTRATION SET, MODEL 21-7090 receive FDA 510(k) clearance?

CADD CHECKVALVE ADMINISTRATION SET, MODEL 21-7090 received FDA 510(k) clearance on 2000-04-27, under 510(k) number K000942.

Who is the listed applicant for CADD CHECKVALVE ADMINISTRATION SET, MODEL 21-7090?

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

What is the FDA product code for CADD CHECKVALVE ADMINISTRATION SET, MODEL 21-7090?

The FDA product code for CADD CHECKVALVE ADMINISTRATION SET, MODEL 21-7090 is FPA.

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 Sims Deltec, 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 32 devices →

Related Devices (Code: FPA)

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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