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FDA 510(k)

LMT ARTHROSCOPIC SUTURING INSTRUMENTS

K-Number: K941964 · 1994-09-28

ApplicantLi Medical Technologies, Inc.
Decision Date1994-09-28
Product CodeHRX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

LMT ARTHROSCOPIC SUTURING INSTRUMENTS is the device name listed in this FDA 510(k) record. The listed applicant is Li Medical Technologies, Inc.. It received FDA 510(k) clearance on 1994-09-28 under 510(k) number K941964. The device is classified under product code HRX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LMT ARTHROSCOPIC SUTURING INSTRUMENTS?

LMT ARTHROSCOPIC SUTURING INSTRUMENTS is a medical device that received FDA 510(k) clearance on 1994-09-28. The listed applicant is Li Medical Technologies, Inc.. The 510(k) number is K941964.

When did LMT ARTHROSCOPIC SUTURING INSTRUMENTS receive FDA 510(k) clearance?

LMT ARTHROSCOPIC SUTURING INSTRUMENTS received FDA 510(k) clearance on 1994-09-28, under 510(k) number K941964.

Who is the listed applicant for LMT ARTHROSCOPIC SUTURING INSTRUMENTS?

The FDA 510(k) record lists Li Medical Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LMT ARTHROSCOPIC SUTURING INSTRUMENTS?

The FDA product code for LMT ARTHROSCOPIC SUTURING INSTRUMENTS is HRX.

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Other records listing Li Medical Technologies, Inc. as applicant

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Related Devices (Code: HRX)

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.

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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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