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FDA 510(k)

KORBER ARTERIOTOMY SCISSORS

K-Number: K884373 · 1988-11-08

ApplicantMicrins, Ltd.
Decision Date1988-11-08
Product CodeLRW
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

KORBER ARTERIOTOMY SCISSORS is the device name listed in this FDA 510(k) record. The listed applicant is Micrins, Ltd.. It received FDA 510(k) clearance on 1988-11-08 under 510(k) number K884373. The device is classified under product code LRW. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KORBER ARTERIOTOMY SCISSORS?

KORBER ARTERIOTOMY SCISSORS is a medical device that received FDA 510(k) clearance on 1988-11-08. The listed applicant is Micrins, Ltd.. The 510(k) number is K884373.

When did KORBER ARTERIOTOMY SCISSORS receive FDA 510(k) clearance?

KORBER ARTERIOTOMY SCISSORS received FDA 510(k) clearance on 1988-11-08, under 510(k) number K884373.

Who is the listed applicant for KORBER ARTERIOTOMY SCISSORS?

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

What is the FDA product code for KORBER ARTERIOTOMY SCISSORS?

The FDA product code for KORBER ARTERIOTOMY SCISSORS is LRW.

Related Clinical Trials

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.

Other records listing Micrins, 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.

Related Devices (Code: LRW)

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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