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FDA 510(k)

SUCTION/IRRIGATION CANNULA; CATLOG #532.00

K-Number: K915298 · 1992-01-23

ApplicantLifeguard Medical Products, Inc.
Decision Date1992-01-23
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

SUCTION/IRRIGATION CANNULA; CATLOG #532.00 is the device name listed in this FDA 510(k) record. The listed applicant is Lifeguard Medical Products, Inc.. It received FDA 510(k) clearance on 1992-01-23 under 510(k) number K915298. 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 SUCTION/IRRIGATION CANNULA; CATLOG #532.00?

SUCTION/IRRIGATION CANNULA; CATLOG #532.00 is a medical device that received FDA 510(k) clearance on 1992-01-23. The listed applicant is Lifeguard Medical Products, Inc.. The 510(k) number is K915298.

When did SUCTION/IRRIGATION CANNULA; CATLOG #532.00 receive FDA 510(k) clearance?

SUCTION/IRRIGATION CANNULA; CATLOG #532.00 received FDA 510(k) clearance on 1992-01-23, under 510(k) number K915298.

Who is the listed applicant for SUCTION/IRRIGATION CANNULA; CATLOG #532.00?

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

What is the FDA product code for SUCTION/IRRIGATION CANNULA; CATLOG #532.00?

The FDA product code for SUCTION/IRRIGATION CANNULA; CATLOG #532.00 is GCJ.

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Other records listing Lifeguard Medical Products, 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.

K013421LIFEGUARD NASAL CPAP MASK AND ACCESSORIESK915296MONOPOLAR ELECTRODEK920471LEVY ARTICULATING RETRACTORK915505REGULATOR FLOWMETERK915297TROCAR & TROCAR SLEEEVE 11MM, 10MM, 8MM & 5MMK880958LIFEGUARD BACTERIAL AND VIRAL FILTER

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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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