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FDA 510(k)

DIDECO D920, LILLIPUT 1 TWIN RESERVOIR

K-Number: K984322 · 1999-03-02

ApplicantDideco S.P.A.
Decision Date1999-03-02
Product CodeDTP
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

DIDECO D920, LILLIPUT 1 TWIN RESERVOIR is the device name listed in this FDA 510(k) record. The listed applicant is Dideco S.P.A.. It received FDA 510(k) clearance on 1999-03-02 under 510(k) number K984322. The device is classified under product code DTP. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DIDECO D920, LILLIPUT 1 TWIN RESERVOIR?

DIDECO D920, LILLIPUT 1 TWIN RESERVOIR is a medical device that received FDA 510(k) clearance on 1999-03-02. The listed applicant is Dideco S.P.A.. The 510(k) number is K984322.

When did DIDECO D920, LILLIPUT 1 TWIN RESERVOIR receive FDA 510(k) clearance?

DIDECO D920, LILLIPUT 1 TWIN RESERVOIR received FDA 510(k) clearance on 1999-03-02, under 510(k) number K984322.

Who is the listed applicant for DIDECO D920, LILLIPUT 1 TWIN RESERVOIR?

The FDA 510(k) record lists Dideco S.P.A. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DIDECO D920, LILLIPUT 1 TWIN RESERVOIR?

The FDA product code for DIDECO D920, LILLIPUT 1 TWIN RESERVOIR is DTP.

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Other records listing Dideco S.P.A. as applicant

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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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