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FDA 510(k)

MCKERNAN ATRAUMATIC FORCEPS

K-Number: K925041 · 1992-11-25

ApplicantAslan Medical Technologies, Ltd.
Decision Date1992-11-25
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MCKERNAN ATRAUMATIC 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 1992-11-25 under 510(k) number K925041. 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 ATRAUMATIC FORCEPS?

MCKERNAN ATRAUMATIC FORCEPS is a medical device that received FDA 510(k) clearance on 1992-11-25. The listed applicant is Aslan Medical Technologies, Ltd.. The 510(k) number is K925041.

When did MCKERNAN ATRAUMATIC FORCEPS receive FDA 510(k) clearance?

MCKERNAN ATRAUMATIC FORCEPS received FDA 510(k) clearance on 1992-11-25, under 510(k) number K925041.

Who is the listed applicant for MCKERNAN ATRAUMATIC 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 ATRAUMATIC FORCEPS?

The FDA product code for MCKERNAN ATRAUMATIC 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)

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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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