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FDA 510(k)

MODIFICATION TO MULTAPORT CANNULA, REDUCER AND ACCESSORIES

K-Number: K990379 · 1999-03-04

ApplicantDexide, Inc.
Decision Date1999-03-04
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MODIFICATION TO MULTAPORT CANNULA, REDUCER AND ACCESSORIES is the device name listed in this FDA 510(k) record. The listed applicant is Dexide, Inc.. It received FDA 510(k) clearance on 1999-03-04 under 510(k) number K990379. 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 MODIFICATION TO MULTAPORT CANNULA, REDUCER AND ACCESSORIES?

MODIFICATION TO MULTAPORT CANNULA, REDUCER AND ACCESSORIES is a medical device that received FDA 510(k) clearance on 1999-03-04. The listed applicant is Dexide, Inc.. The 510(k) number is K990379.

When did MODIFICATION TO MULTAPORT CANNULA, REDUCER AND ACCESSORIES receive FDA 510(k) clearance?

MODIFICATION TO MULTAPORT CANNULA, REDUCER AND ACCESSORIES received FDA 510(k) clearance on 1999-03-04, under 510(k) number K990379.

Who is the listed applicant for MODIFICATION TO MULTAPORT CANNULA, REDUCER AND ACCESSORIES?

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 MODIFICATION TO MULTAPORT CANNULA, REDUCER AND ACCESSORIES?

The FDA product code for MODIFICATION TO MULTAPORT CANNULA, REDUCER AND ACCESSORIES is GCJ.

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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 INSTRUMENTSK981940MULTAPUMP DISPOSABLE PUMP HEAD AND ACCESSORIESK981941MULTAPORT CANNULA REDUCER AND ACCESSORIESK953611DEXIDE ENDO-LUBE KITK944509DEXIDE INSUFFLATION TUBING WITH FILTERK924117DEXIDE LAPAROSCOPIC KITS

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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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