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FDA 510(k)

STD IRRIGATION PUMP

K-Number: K930427 · 1993-06-01

ApplicantStd Mfg., Inc.
Decision Date1993-06-01
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

STD IRRIGATION PUMP is the device name listed in this FDA 510(k) record. The listed applicant is Std Mfg., Inc.. It received FDA 510(k) clearance on 1993-06-01 under 510(k) number K930427. 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 STD IRRIGATION PUMP?

STD IRRIGATION PUMP is a medical device that received FDA 510(k) clearance on 1993-06-01. The listed applicant is Std Mfg., Inc.. The 510(k) number is K930427.

When did STD IRRIGATION PUMP receive FDA 510(k) clearance?

STD IRRIGATION PUMP received FDA 510(k) clearance on 1993-06-01, under 510(k) number K930427.

Who is the listed applicant for STD IRRIGATION PUMP?

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

What is the FDA product code for STD IRRIGATION PUMP?

The FDA product code for STD IRRIGATION PUMP 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 Std Mfg., 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.

K023096CONTOURED ARTICULAR PROSTHESIS (CAP) HUMERAL HEAD RESURFACING SYSTEMK021549CONTOURED ARTICULAR PROSTHESIS (CAP) FEMORAL HEAD RESURFACING SYSTEMK012362MODIFICATION TO VASCULAR CLOSURE DEVICEK003169VASCULAR CLOSURE DEVICEK000608SUCTION VASCULAR STAPLER AND IMPLANTABLE STAPLE SYSTEM

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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