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FDA 510(k)

CIPA (ADULTS) CIPI (INFANTS)

K-Number: K992932 · 2000-06-07

ApplicantDmc Medical, Ltd.
Decision Date2000-06-07
Product CodeDWF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CIPA (ADULTS) CIPI (INFANTS) is the device name listed in this FDA 510(k) record. The listed applicant is Dmc Medical, Ltd.. It received FDA 510(k) clearance on 2000-06-07 under 510(k) number K992932. The device is classified under product code DWF. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CIPA (ADULTS) CIPI (INFANTS)?

CIPA (ADULTS) CIPI (INFANTS) is a medical device that received FDA 510(k) clearance on 2000-06-07. The listed applicant is Dmc Medical, Ltd.. The 510(k) number is K992932.

When did CIPA (ADULTS) CIPI (INFANTS) receive FDA 510(k) clearance?

CIPA (ADULTS) CIPI (INFANTS) received FDA 510(k) clearance on 2000-06-07, under 510(k) number K992932.

Who is the listed applicant for CIPA (ADULTS) CIPI (INFANTS)?

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

What is the FDA product code for CIPA (ADULTS) CIPI (INFANTS)?

The FDA product code for CIPA (ADULTS) CIPI (INFANTS) is DWF.

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Other records listing Dmc Medical, Ltd. 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.

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Related Devices (Code: DWF)

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.

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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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