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FDA 510(k)

MOORE TYPE ENDO PROSTHESIS

K-Number: K900051 · 1990-10-03

ApplicantLima Intl. Corp.
Decision Date1990-10-03
Product CodeKWY
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MOORE TYPE ENDO PROSTHESIS is the device name listed in this FDA 510(k) record. The listed applicant is Lima Intl. Corp.. It received FDA 510(k) clearance on 1990-10-03 under 510(k) number K900051. The device is classified under product code KWY. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MOORE TYPE ENDO PROSTHESIS?

MOORE TYPE ENDO PROSTHESIS is a medical device that received FDA 510(k) clearance on 1990-10-03. The listed applicant is Lima Intl. Corp.. The 510(k) number is K900051.

When did MOORE TYPE ENDO PROSTHESIS receive FDA 510(k) clearance?

MOORE TYPE ENDO PROSTHESIS received FDA 510(k) clearance on 1990-10-03, under 510(k) number K900051.

Who is the listed applicant for MOORE TYPE ENDO PROSTHESIS?

The FDA 510(k) record lists Lima Intl. Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MOORE TYPE ENDO PROSTHESIS?

The FDA product code for MOORE TYPE ENDO PROSTHESIS is KWY.

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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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