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FDA 510(k)

DC-1 I.V. DOSAGE COMPUTER

K-Number: K884016 · 1988-12-20

ApplicantPhase Medical, Inc.
Decision Date1988-12-20
Product CodeNDC
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

DC-1 I.V. DOSAGE COMPUTER is the device name listed in this FDA 510(k) record. The listed applicant is Phase Medical, Inc.. It received FDA 510(k) clearance on 1988-12-20 under 510(k) number K884016. The device is classified under product code NDC. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DC-1 I.V. DOSAGE COMPUTER?

DC-1 I.V. DOSAGE COMPUTER is a medical device that received FDA 510(k) clearance on 1988-12-20. The listed applicant is Phase Medical, Inc.. The 510(k) number is K884016.

When did DC-1 I.V. DOSAGE COMPUTER receive FDA 510(k) clearance?

DC-1 I.V. DOSAGE COMPUTER received FDA 510(k) clearance on 1988-12-20, under 510(k) number K884016.

Who is the listed applicant for DC-1 I.V. DOSAGE COMPUTER?

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

What is the FDA product code for DC-1 I.V. DOSAGE COMPUTER?

The FDA product code for DC-1 I.V. DOSAGE COMPUTER is NDC.

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Related Devices (Code: NDC)

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.

K254102GlucommanderGlytec, LLCK260910EndoTool IV Cloud 1.0Glooko, Inc.K253512MiniMed Go AppMedtronic MinimedK253281UpDocUpdoc, Inc.K252104T1D1Comerge AGK241088EndoTool IV (3.1)Monarch Medical Technologies

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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