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FDA 510(k)

MCKERNAN-ADSON AGGRESSIVE FORCEPS

K-Number: K926281 · 1993-03-09

ApplicantAslan Medical Technologies, Ltd.
Decision Date1993-03-09
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MCKERNAN-ADSON AGGRESSIVE FORCEPS is the device name listed in this FDA 510(k) record. The listed applicant is Aslan Medical Technologies, Ltd.. It received FDA 510(k) clearance on 1993-03-09 under 510(k) number K926281. 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 MCKERNAN-ADSON AGGRESSIVE FORCEPS?

MCKERNAN-ADSON AGGRESSIVE FORCEPS is a medical device that received FDA 510(k) clearance on 1993-03-09. The listed applicant is Aslan Medical Technologies, Ltd.. The 510(k) number is K926281.

When did MCKERNAN-ADSON AGGRESSIVE FORCEPS receive FDA 510(k) clearance?

MCKERNAN-ADSON AGGRESSIVE FORCEPS received FDA 510(k) clearance on 1993-03-09, under 510(k) number K926281.

Who is the listed applicant for MCKERNAN-ADSON AGGRESSIVE FORCEPS?

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

What is the FDA product code for MCKERNAN-ADSON AGGRESSIVE FORCEPS?

The FDA product code for MCKERNAN-ADSON AGGRESSIVE FORCEPS is GCJ.

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Other records listing Aslan Medical Technologies, 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.

K982287ASLAN SENSOR MODULAR INSTRUMENTK954864ASLAN MODULAR INSTRUMENTK952264ASLAN LAPRETRACTK950924ASLAN KNOT PUSHERK944082ASLAN DUAL ACTION JAWS GRASPING FORCEPSK926282MCKERNAN-POTTS GRASPING FORCEPS

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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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