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FDA 510(k)

ASLAN MODULAR INSTRUMENT

K-Number: K954864 · 1996-02-09

ApplicantAslan Medical Technologies, Ltd.
Decision Date1996-02-09
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ASLAN MODULAR INSTRUMENT 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 1996-02-09 under 510(k) number K954864. 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 ASLAN MODULAR INSTRUMENT?

ASLAN MODULAR INSTRUMENT is a medical device that received FDA 510(k) clearance on 1996-02-09. The listed applicant is Aslan Medical Technologies, Ltd.. The 510(k) number is K954864.

When did ASLAN MODULAR INSTRUMENT receive FDA 510(k) clearance?

ASLAN MODULAR INSTRUMENT received FDA 510(k) clearance on 1996-02-09, under 510(k) number K954864.

Who is the listed applicant for ASLAN MODULAR INSTRUMENT?

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 ASLAN MODULAR INSTRUMENT?

The FDA product code for ASLAN MODULAR INSTRUMENT 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 INSTRUMENTK952264ASLAN LAPRETRACTK950924ASLAN KNOT PUSHERK944082ASLAN DUAL ACTION JAWS GRASPING FORCEPSK926281MCKERNAN-ADSON AGGRESSIVE 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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