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FDA 510(k)

DP-700 NIKMAN DEFIB-PADS

K-Number: K872793 · 1987-10-09

ApplicantNikomed U.S.A., Inc.
Decision Date1987-10-09
Product CodeLDD
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

DP-700 NIKMAN DEFIB-PADS is the device name listed in this FDA 510(k) record. The listed applicant is Nikomed U.S.A., Inc.. It received FDA 510(k) clearance on 1987-10-09 under 510(k) number K872793. The device is classified under product code LDD. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DP-700 NIKMAN DEFIB-PADS?

DP-700 NIKMAN DEFIB-PADS is a medical device that received FDA 510(k) clearance on 1987-10-09. The listed applicant is Nikomed U.S.A., Inc.. The 510(k) number is K872793.

When did DP-700 NIKMAN DEFIB-PADS receive FDA 510(k) clearance?

DP-700 NIKMAN DEFIB-PADS received FDA 510(k) clearance on 1987-10-09, under 510(k) number K872793.

Who is the listed applicant for DP-700 NIKMAN DEFIB-PADS?

The FDA 510(k) record lists Nikomed U.S.A., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DP-700 NIKMAN DEFIB-PADS?

The FDA product code for DP-700 NIKMAN DEFIB-PADS is LDD.

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Related Devices (Code: LDD)

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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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