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FDA 510(k)

LAPORASCOPIC CANNULA SEAL

K-Number: K933025 · 1994-01-25

ApplicantLi Medical Technologies, Inc.
Decision Date1994-01-25
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

LAPORASCOPIC CANNULA SEAL 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 1994-01-25 under 510(k) number K933025. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LAPORASCOPIC CANNULA SEAL?

LAPORASCOPIC CANNULA SEAL is a medical device that received FDA 510(k) clearance on 1994-01-25. The listed applicant is Li Medical Technologies, Inc.. The 510(k) number is K933025.

When did LAPORASCOPIC CANNULA SEAL receive FDA 510(k) clearance?

LAPORASCOPIC CANNULA SEAL received FDA 510(k) clearance on 1994-01-25, under 510(k) number K933025.

Who is the listed applicant for LAPORASCOPIC CANNULA SEAL?

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 LAPORASCOPIC CANNULA SEAL?

The FDA product code for LAPORASCOPIC CANNULA SEAL is GCJ.

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Other records listing Li Medical Technologies, Inc. as applicant

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Related Devices (Code: GCJ)

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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