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FDA 510(k)

CA GUARD, LTD. PSP (PORT SITE PROTECTOR)

K-Number: K992182 · 2000-07-18

ApplicantCa Guard, Ltd.
Decision Date2000-07-18
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

CA GUARD, LTD. PSP (PORT SITE PROTECTOR) is the device name listed in this FDA 510(k) record. The listed applicant is Ca Guard, Ltd.. It received FDA 510(k) clearance on 2000-07-18 under 510(k) number K992182. 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 CA GUARD, LTD. PSP (PORT SITE PROTECTOR)?

CA GUARD, LTD. PSP (PORT SITE PROTECTOR) is a medical device that received FDA 510(k) clearance on 2000-07-18. The listed applicant is Ca Guard, Ltd.. The 510(k) number is K992182.

When did CA GUARD, LTD. PSP (PORT SITE PROTECTOR) receive FDA 510(k) clearance?

CA GUARD, LTD. PSP (PORT SITE PROTECTOR) received FDA 510(k) clearance on 2000-07-18, under 510(k) number K992182.

Who is the listed applicant for CA GUARD, LTD. PSP (PORT SITE PROTECTOR)?

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

What is the FDA product code for CA GUARD, LTD. PSP (PORT SITE PROTECTOR)?

The FDA product code for CA GUARD, LTD. PSP (PORT SITE PROTECTOR) 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 Ca Guard, Ltd. 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.

K020614IRRIGATING CANNULA

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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