FDA 510(k)

LUNAPADS

K-Number: K010986 · 2001-06-13

ApplicantLunapads International Products, Ltd.

Decision Date2001-06-13

Product CodeNUQ

Advisory CommitteeOB

DecisionSubstantially Equivalent

Device Summary

LUNAPADS is the device name listed in this FDA 510(k) record. The listed applicant is Lunapads International Products, Ltd.. It received FDA 510(k) clearance on 2001-06-13 under 510(k) number K010986. The device is classified under product code NUQ. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LUNAPADS?

LUNAPADS is a medical device that received FDA 510(k) clearance on 2001-06-13. The listed applicant is Lunapads International Products, Ltd.. The 510(k) number is K010986.

When did LUNAPADS receive FDA 510(k) clearance?

LUNAPADS received FDA 510(k) clearance on 2001-06-13, under 510(k) number K010986.

Who is the listed applicant for LUNAPADS?

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

What is the FDA product code for LUNAPADS?

The FDA product code for LUNAPADS is NUQ.

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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.