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FDA 510(k)

ASLAN KNOT PUSHER

K-Number: K950924 · 1995-03-14

ApplicantAslan Medical Technologies, Ltd.
Decision Date1995-03-14
Product CodeFDE
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ASLAN KNOT PUSHER 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 1995-03-14 under 510(k) number K950924. The device is classified under product code FDE. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ASLAN KNOT PUSHER?

ASLAN KNOT PUSHER is a medical device that received FDA 510(k) clearance on 1995-03-14. The listed applicant is Aslan Medical Technologies, Ltd.. The 510(k) number is K950924.

When did ASLAN KNOT PUSHER receive FDA 510(k) clearance?

ASLAN KNOT PUSHER received FDA 510(k) clearance on 1995-03-14, under 510(k) number K950924.

Who is the listed applicant for ASLAN KNOT PUSHER?

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 KNOT PUSHER?

The FDA product code for ASLAN KNOT PUSHER is FDE.

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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 LAPRETRACTK944082ASLAN DUAL ACTION JAWS GRASPING FORCEPSK926281MCKERNAN-ADSON AGGRESSIVE FORCEPSK926282MCKERNAN-POTTS GRASPING FORCEPS

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Related Devices (Code: FDE)

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.

K955717ENDOSCOPE INTRODUCER KITMitsubishi Cable America, Inc.K942677GEENEN/ZEBRA GUIDELINESBoston Scientific CorpK912443CANDELA INTRODUCER SHEATH SYSTEMCandela Laser Corp.

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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