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FDA 510(k)

MONOSCOPY BRAND, 5 MM LOCKING TROCAR SLEEVE

K-Number: K896205 · 1990-03-22

ApplicantDexide, Inc.
Decision Date1990-03-22
Product CodeGCI
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MONOSCOPY BRAND, 5 MM LOCKING TROCAR SLEEVE is the device name listed in this FDA 510(k) record. The listed applicant is Dexide, Inc.. It received FDA 510(k) clearance on 1990-03-22 under 510(k) number K896205. The device is classified under product code GCI. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MONOSCOPY BRAND, 5 MM LOCKING TROCAR SLEEVE?

MONOSCOPY BRAND, 5 MM LOCKING TROCAR SLEEVE is a medical device that received FDA 510(k) clearance on 1990-03-22. The listed applicant is Dexide, Inc.. The 510(k) number is K896205.

When did MONOSCOPY BRAND, 5 MM LOCKING TROCAR SLEEVE receive FDA 510(k) clearance?

MONOSCOPY BRAND, 5 MM LOCKING TROCAR SLEEVE received FDA 510(k) clearance on 1990-03-22, under 510(k) number K896205.

Who is the listed applicant for MONOSCOPY BRAND, 5 MM LOCKING TROCAR SLEEVE?

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

What is the FDA product code for MONOSCOPY BRAND, 5 MM LOCKING TROCAR SLEEVE?

The FDA product code for MONOSCOPY BRAND, 5 MM LOCKING TROCAR SLEEVE is GCI.

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Other records listing Dexide, Inc. as applicant

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.

K991814MULTACHOICE INSTRUMENTSK990379MODIFICATION TO MULTAPORT CANNULA, REDUCER AND ACCESSORIESK981940MULTAPUMP DISPOSABLE PUMP HEAD AND ACCESSORIESK981941MULTAPORT CANNULA REDUCER AND ACCESSORIESK953611DEXIDE ENDO-LUBE KITK944509DEXIDE INSUFFLATION TUBING WITH FILTER

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Related Devices (Code: GCI)

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.

K021747DEGALL LAPAROSCOPIC GALLBLADDER EXTRACTORSurgicon, Inc.K003222MODIFICATION TO HERMES OPERATING ROOM CONTROL CENTERComputer Motion, Inc.K001362KARL STORZ 3D VIDEO SYSTEMKarl Storz Imaging, Inc.K933515BOOTY ENDOSCOPE WARMERT-Med, Inc.K930302BIRTCHER SURE CLEAN INSTRUMENT SYSTEMBirtcher Medical Systems, Inc.K930496GI-1090,1095,1080,1085,1086,1088, ENDO. CLAMPSBirtcher Medical Systems, Inc.

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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