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FDA 510(k)

ACCESS SURGICAL INT'L ENDOSCOPIC SURGICAL INSTRUM.

K-Number: K922424 · 1992-11-25

ApplicantAccess Surgical Intl., Inc.
Decision Date1992-11-25
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ACCESS SURGICAL INT'L ENDOSCOPIC SURGICAL INSTRUM. is the device name listed in this FDA 510(k) record. The listed applicant is Access Surgical Intl., Inc.. It received FDA 510(k) clearance on 1992-11-25 under 510(k) number K922424. 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 ACCESS SURGICAL INT'L ENDOSCOPIC SURGICAL INSTRUM.?

ACCESS SURGICAL INT'L ENDOSCOPIC SURGICAL INSTRUM. is a medical device that received FDA 510(k) clearance on 1992-11-25. The listed applicant is Access Surgical Intl., Inc.. The 510(k) number is K922424.

When did ACCESS SURGICAL INT'L ENDOSCOPIC SURGICAL INSTRUM. receive FDA 510(k) clearance?

ACCESS SURGICAL INT'L ENDOSCOPIC SURGICAL INSTRUM. received FDA 510(k) clearance on 1992-11-25, under 510(k) number K922424.

Who is the listed applicant for ACCESS SURGICAL INT'L ENDOSCOPIC SURGICAL INSTRUM.?

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

What is the FDA product code for ACCESS SURGICAL INT'L ENDOSCOPIC SURGICAL INSTRUM.?

The FDA product code for ACCESS SURGICAL INT'L ENDOSCOPIC SURGICAL INSTRUM. is GCJ.

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Other records listing Access Surgical Intl., 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.

K954536BLADE, SCALPEL & BLADE, HANDELK953376ACCESS POINTK945545ACCESS SURGICAL INT'L THORACIC ENDOSCOPIC SURGICAL INSTRUMENTSK944974ACCESS POINTK940587FLEX-I-PORTK933192ACCESS SURGICAL INT'L INC. ENDOSCOPIC SURG. INST.

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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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