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FDA 510(k)

MULTAPUMP DISPOSABLE PUMP HEAD AND ACCESSORIES

K-Number: K981940 · 1998-09-25

ApplicantDexide, Inc.
Decision Date1998-09-25
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MULTAPUMP DISPOSABLE PUMP HEAD 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 1998-09-25 under 510(k) number K981940. 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 MULTAPUMP DISPOSABLE PUMP HEAD AND ACCESSORIES?

MULTAPUMP DISPOSABLE PUMP HEAD AND ACCESSORIES is a medical device that received FDA 510(k) clearance on 1998-09-25. The listed applicant is Dexide, Inc.. The 510(k) number is K981940.

When did MULTAPUMP DISPOSABLE PUMP HEAD AND ACCESSORIES receive FDA 510(k) clearance?

MULTAPUMP DISPOSABLE PUMP HEAD AND ACCESSORIES received FDA 510(k) clearance on 1998-09-25, under 510(k) number K981940.

Who is the listed applicant for MULTAPUMP DISPOSABLE PUMP HEAD 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 MULTAPUMP DISPOSABLE PUMP HEAD AND ACCESSORIES?

The FDA product code for MULTAPUMP DISPOSABLE PUMP HEAD 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 INSTRUMENTSK990379MODIFICATION TO MULTAPORT CANNULA, REDUCER 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.

K262397CuratOR EX2742Eizo CorporationK260884UNIDRIVE Select SystemKarl Storz SE & CO. KGK260972OEV-271MUH LCD Monitor;OEV-321MUH LCD Monitor;OEV-431MUH LCD MonitorSony CorporationK261139VereSee (VER150, VER200, VER151, VER201, VER200C, and VER-100-103)Freyja Healthcare, LLCK253541EZ-Close™ (EZ Close Port Site Closing Device, EZ Close MAX Port Site Closing Device, EZ Close II Port Site Closing Device)Medical ImpactK261614LED LCD Monitor (OEV-271H)Lg Electronics.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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