FDA 510(k)

MEDICON INSTRUMENTS TROCARS, TROCAR SLEEVES AND REDUCTION SLEEVES

K-Number: K936247 · 1994-05-19

Decision Date1994-05-19

Product CodeDRC

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

MEDICON INSTRUMENTS TROCARS, TROCAR SLEEVES AND REDUCTION SLEEVES is the device name listed in this FDA 510(k) record. The listed applicant is Medicon Instruments, Inc.. It received FDA 510(k) clearance on 1994-05-19 under 510(k) number K936247. The device is classified under product code DRC. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDICON INSTRUMENTS TROCARS, TROCAR SLEEVES AND REDUCTION SLEEVES?

MEDICON INSTRUMENTS TROCARS, TROCAR SLEEVES AND REDUCTION SLEEVES is a medical device that received FDA 510(k) clearance on 1994-05-19. The listed applicant is Medicon Instruments, Inc.. The 510(k) number is K936247.

When did MEDICON INSTRUMENTS TROCARS, TROCAR SLEEVES AND REDUCTION SLEEVES receive FDA 510(k) clearance?

MEDICON INSTRUMENTS TROCARS, TROCAR SLEEVES AND REDUCTION SLEEVES received FDA 510(k) clearance on 1994-05-19, under 510(k) number K936247.

Who is the listed applicant for MEDICON INSTRUMENTS TROCARS, TROCAR SLEEVES AND REDUCTION SLEEVES?

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

What is the FDA product code for MEDICON INSTRUMENTS TROCARS, TROCAR SLEEVES AND REDUCTION SLEEVES?

The FDA product code for MEDICON INSTRUMENTS TROCARS, TROCAR SLEEVES AND REDUCTION SLEEVES is DRC.

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Other records listing Medicon Instruments, Inc. as applicant

K936249MEDICON INSTRUMENTS UNIPOLAR COAGULATION ELECTRODES K936246MEDICON INSTRUMENTS BIPOLAR FORCEPTS AND ELECTRODES K936262DISSECTORS, FORCEPS, SCISSORS, DILATION SETS, AND GALL STONE COLLECTORS K936248MEDICON INSTRUMENTS CHOLANGIOGRAPHY NEEDLES, GUIDE TUBES, INJECTION NEEDLES, VERRES INSUFFLATION NEEDLES AND HOLDERS K936250RETRACTORS, SPECULUM, CLIP APPLIER FOR TITANIUM CLIPS, 2-WAY STOP COCK, PALPATION PROBE, KNOT GUIDE, ROEDER LOOP

Related Devices (Code: DRC)

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.