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FDA 510(k)

QUICK SWITCH LAPAROSCOPIC INSTRUMENTS

K-Number: K932648 · 1993-10-12

ApplicantMicroline Pentax, Inc.
Decision Date1993-10-12
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

QUICK SWITCH LAPAROSCOPIC INSTRUMENTS is the device name listed in this FDA 510(k) record. The listed applicant is Microline Pentax, Inc.. It received FDA 510(k) clearance on 1993-10-12 under 510(k) number K932648. 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 QUICK SWITCH LAPAROSCOPIC INSTRUMENTS?

QUICK SWITCH LAPAROSCOPIC INSTRUMENTS is a medical device that received FDA 510(k) clearance on 1993-10-12. The listed applicant is Microline Pentax, Inc.. The 510(k) number is K932648.

When did QUICK SWITCH LAPAROSCOPIC INSTRUMENTS receive FDA 510(k) clearance?

QUICK SWITCH LAPAROSCOPIC INSTRUMENTS received FDA 510(k) clearance on 1993-10-12, under 510(k) number K932648.

Who is the listed applicant for QUICK SWITCH LAPAROSCOPIC INSTRUMENTS?

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

What is the FDA product code for QUICK SWITCH LAPAROSCOPIC INSTRUMENTS?

The FDA product code for QUICK SWITCH LAPAROSCOPIC INSTRUMENTS is GCJ.

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Other records listing Microline Pentax, 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.

K013695MICROLINE INC. REUSABLE LAPAROSCOPIC CLIP APPLIER WITH IMPLANTABLE TITANIUM CLIPS, MODEL M/L-10K982984ACCUSHEAR LAPAROSCOPIC SURGICAL INSTRUMENTSK981389DISPOSABLE RE-NEW FORCEPSK981188ELECTROSURGICAL CAUTERY PROBESK9807583 MM SELEC-TIP LAPAROSCOPIC SCISSORSK974066RE-NEW FORCEPS LAPAROSCOPIC SURGICAL TIPS

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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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