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FDA 510(k)

10.0MM SUCTION/IRRIGATION PROBE & TUBING KIT

K-Number: K932805 · 1993-08-16

ApplicantMayaguez Medical Center
Decision Date1993-08-16
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

10.0MM SUCTION/IRRIGATION PROBE & TUBING KIT is the device name listed in this FDA 510(k) record. The listed applicant is Mayaguez Medical Center. It received FDA 510(k) clearance on 1993-08-16 under 510(k) number K932805. 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 10.0MM SUCTION/IRRIGATION PROBE & TUBING KIT?

10.0MM SUCTION/IRRIGATION PROBE & TUBING KIT is a medical device that received FDA 510(k) clearance on 1993-08-16. The listed applicant is Mayaguez Medical Center. The 510(k) number is K932805.

When did 10.0MM SUCTION/IRRIGATION PROBE & TUBING KIT receive FDA 510(k) clearance?

10.0MM SUCTION/IRRIGATION PROBE & TUBING KIT received FDA 510(k) clearance on 1993-08-16, under 510(k) number K932805.

Who is the listed applicant for 10.0MM SUCTION/IRRIGATION PROBE & TUBING KIT?

The FDA 510(k) record lists Mayaguez Medical Center as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for 10.0MM SUCTION/IRRIGATION PROBE & TUBING KIT?

The FDA product code for 10.0MM SUCTION/IRRIGATION PROBE & TUBING KIT is GCJ.

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Other records listing Mayaguez Medical Center 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.

K932804IRRIGATING TAPERED PROBEK932806POOLE TIP SUCTION PROBE & TUBING KITK931950POOLE TIP SUCTION PROBEK931854ENDOSCOPIC BLUNT DISSECTING INSTRUMENTK931912IRRIGATING BLUNT DISSECTORK9318565.0 MM IRRIGATION/ASPIRATION PROBE

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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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