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FDA 510(k)

LOCKING PIVOTAL THORACOPORT

K-Number: K930463 · 1993-09-07

ApplicantSurgical Technologies, Inc.
Decision Date1993-09-07
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

LOCKING PIVOTAL THORACOPORT is the device name listed in this FDA 510(k) record. The listed applicant is Surgical Technologies, Inc.. It received FDA 510(k) clearance on 1993-09-07 under 510(k) number K930463. 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 LOCKING PIVOTAL THORACOPORT?

LOCKING PIVOTAL THORACOPORT is a medical device that received FDA 510(k) clearance on 1993-09-07. The listed applicant is Surgical Technologies, Inc.. The 510(k) number is K930463.

When did LOCKING PIVOTAL THORACOPORT receive FDA 510(k) clearance?

LOCKING PIVOTAL THORACOPORT received FDA 510(k) clearance on 1993-09-07, under 510(k) number K930463.

Who is the listed applicant for LOCKING PIVOTAL THORACOPORT?

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

What is the FDA product code for LOCKING PIVOTAL THORACOPORT?

The FDA product code for LOCKING PIVOTAL THORACOPORT is GCJ.

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Other records listing Surgical Technologies, 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.

K941992CYSTOSCOPEK942029ARTHROSCOPEK946136INFINITECH LIGHTED INFUSION CANNULAK952566OSCILFLATORK951918SURGICAL TECHNOLOGIES, INC. SYRINGEK950683ARTHROGRAM TRAY

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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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