FDA 510(k)

OVERTUBE FOR ENDSCOPIC LIGATOR

K-Number: K924764 · 1993-03-15

ApplicantSuperior Healthcare Group, Inc.

Decision Date1993-03-15

Product CodeMNK

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

OVERTUBE FOR ENDSCOPIC LIGATOR is the device name listed in this FDA 510(k) record. The listed applicant is Superior Healthcare Group, Inc.. It received FDA 510(k) clearance on 1993-03-15 under 510(k) number K924764. The device is classified under product code MNK. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OVERTUBE FOR ENDSCOPIC LIGATOR?

OVERTUBE FOR ENDSCOPIC LIGATOR is a medical device that received FDA 510(k) clearance on 1993-03-15. The listed applicant is Superior Healthcare Group, Inc.. The 510(k) number is K924764.

When did OVERTUBE FOR ENDSCOPIC LIGATOR receive FDA 510(k) clearance?

OVERTUBE FOR ENDSCOPIC LIGATOR received FDA 510(k) clearance on 1993-03-15, under 510(k) number K924764.

Who is the listed applicant for OVERTUBE FOR ENDSCOPIC LIGATOR?

The FDA 510(k) record lists Superior Healthcare Group, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for OVERTUBE FOR ENDSCOPIC LIGATOR?

The FDA product code for OVERTUBE FOR ENDSCOPIC LIGATOR is MNK.

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Other records listing Superior Healthcare Group, Inc. as applicant

K925530INSTRUMENT WARMER K905755NON-STERILE PATIENT EXAMINATION GLOVES K903347SODIUM CHLORIDE SOLUTION K904216STERILE WATER SOLUTION CATALOG # 10000 K903340STERILE URETHRAL CATHETER PROCEDURE KITS K896321NO. 34100 - 8 FR & NO. 34400 - 14 FR CLOSED TRACH.

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Related Devices (Code: MNK)

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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.