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FDA 510(k)

REICH SUCTION/IRRIGATION CANNULA

K-Number: K911164 · 1991-07-05

ApplicantMarlo Surgical Technology
Decision Date1991-07-05
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

REICH SUCTION/IRRIGATION CANNULA is the device name listed in this FDA 510(k) record. The listed applicant is Marlo Surgical Technology. It received FDA 510(k) clearance on 1991-07-05 under 510(k) number K911164. 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 REICH SUCTION/IRRIGATION CANNULA?

REICH SUCTION/IRRIGATION CANNULA is a medical device that received FDA 510(k) clearance on 1991-07-05. The listed applicant is Marlo Surgical Technology. The 510(k) number is K911164.

When did REICH SUCTION/IRRIGATION CANNULA receive FDA 510(k) clearance?

REICH SUCTION/IRRIGATION CANNULA received FDA 510(k) clearance on 1991-07-05, under 510(k) number K911164.

Who is the listed applicant for REICH SUCTION/IRRIGATION CANNULA?

The FDA 510(k) record lists Marlo Surgical Technology as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for REICH SUCTION/IRRIGATION CANNULA?

The FDA product code for REICH SUCTION/IRRIGATION CANNULA is GCJ.

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Other records listing Marlo Surgical Technology 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.

K960810BALLOON CANNULA 15MM X 35MM,15MM X 55MM, 10/12MM X 55MM,10/12MM X 35MM,5MM X 35MM,2MM X 35MMK962273MALLEABLE STYLET 18 CM ME1816ST, 23 CM ME1816NSTK924611IRRIGATION PUMP AND TUBING SETK932634NU-TIP(TM) FORCEPS:GRASPERS/DISSECTORS/SUTURESK932832PRIMUS INSULATED FORCEPSK920611MARLOW LAPAROSCOPIC GRASPING FORCEP

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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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