FDA 510(k)

DPD-12PCC

K-Number: K990734 · 1999-05-28

Decision Date1999-05-28

Product CodeIYE

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

DPD-12PCC is the device name listed in this FDA 510(k) record. The listed applicant is Scanditronix Medical AB. It received FDA 510(k) clearance on 1999-05-28 under 510(k) number K990734. The device is classified under product code IYE. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DPD-12PCC?

DPD-12PCC is a medical device that received FDA 510(k) clearance on 1999-05-28. The listed applicant is Scanditronix Medical AB. The 510(k) number is K990734.

When did DPD-12PCC receive FDA 510(k) clearance?

DPD-12PCC received FDA 510(k) clearance on 1999-05-28, under 510(k) number K990734.

Who is the listed applicant for DPD-12PCC?

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

What is the FDA product code for DPD-12PCC?

The FDA product code for DPD-12PCC is IYE.

Other records listing Scanditronix Medical AB 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.

K011763OMNIDOS K002051INVIDOS K961400RFA-300, LDA UTILITY

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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.