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FDA 510(k)

INNERVISION INC. CANNULA/TROCAR,MULTIPLE TYPES

K-Number: K940731 · 1994-09-13

ApplicantInnervision, Inc.
Decision Date1994-09-13
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

INNERVISION INC. CANNULA/TROCAR,MULTIPLE TYPES is the device name listed in this FDA 510(k) record. The listed applicant is Innervision, Inc.. It received FDA 510(k) clearance on 1994-09-13 under 510(k) number K940731. 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 INNERVISION INC. CANNULA/TROCAR,MULTIPLE TYPES?

INNERVISION INC. CANNULA/TROCAR,MULTIPLE TYPES is a medical device that received FDA 510(k) clearance on 1994-09-13. The listed applicant is Innervision, Inc.. The 510(k) number is K940731.

When did INNERVISION INC. CANNULA/TROCAR,MULTIPLE TYPES receive FDA 510(k) clearance?

INNERVISION INC. CANNULA/TROCAR,MULTIPLE TYPES received FDA 510(k) clearance on 1994-09-13, under 510(k) number K940731.

Who is the listed applicant for INNERVISION INC. CANNULA/TROCAR,MULTIPLE TYPES?

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

What is the FDA product code for INNERVISION INC. CANNULA/TROCAR,MULTIPLE TYPES?

The FDA product code for INNERVISION INC. CANNULA/TROCAR,MULTIPLE TYPES is GCJ.

Related Clinical Trials

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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Other records listing Innervision, 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.

K992345CHRISTOUDIAS SLIM TIP ELECTRODE INSERTK991877MACMED PAEDIATRIC INTRAMEDULLARY NAILK982428CHRISTOUDIAS GAUZE DISSECTOR (LAPAROSCOPIC HAND INSTRUMENT)K940750INNERVISION,INC. LAPAROSCOPIC ELECTRODESK940718INNERVISION INC. LAPAROSCOPIC HAND INSTRUMENTS

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

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

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