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FDA 510(k)

LIMA RPS SHOULDER

K-Number: K913282 · 1991-10-21

ApplicantTurnkey Intergration USA, Inc.
Decision Date1991-10-21
Product CodeHSD
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

LIMA RPS SHOULDER is the device name listed in this FDA 510(k) record. The listed applicant is Turnkey Intergration USA, Inc.. It received FDA 510(k) clearance on 1991-10-21 under 510(k) number K913282. The device is classified under product code HSD. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIMA RPS SHOULDER?

LIMA RPS SHOULDER is a medical device that received FDA 510(k) clearance on 1991-10-21. The listed applicant is Turnkey Intergration USA, Inc.. The 510(k) number is K913282.

When did LIMA RPS SHOULDER receive FDA 510(k) clearance?

LIMA RPS SHOULDER received FDA 510(k) clearance on 1991-10-21, under 510(k) number K913282.

Who is the listed applicant for LIMA RPS SHOULDER?

The FDA 510(k) record lists Turnkey Intergration USA, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LIMA RPS SHOULDER?

The FDA product code for LIMA RPS SHOULDER is HSD.

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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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