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FDA 510(k)

5 STRAIGHT SCISSORS

K-Number: K901169 · 1990-04-16

Decision Date1990-04-16
Product CodeEKJ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

5 STRAIGHT SCISSORS is the device name listed in this FDA 510(k) record. The listed applicant is American Medical Ceramics, Inc.. It received FDA 510(k) clearance on 1990-04-16 under 510(k) number K901169. The device is classified under product code EKJ. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 5 STRAIGHT SCISSORS?

5 STRAIGHT SCISSORS is a medical device that received FDA 510(k) clearance on 1990-04-16. The listed applicant is American Medical Ceramics, Inc.. The 510(k) number is K901169.

When did 5 STRAIGHT SCISSORS receive FDA 510(k) clearance?

5 STRAIGHT SCISSORS received FDA 510(k) clearance on 1990-04-16, under 510(k) number K901169.

Who is the listed applicant for 5 STRAIGHT SCISSORS?

The FDA 510(k) record lists American Medical Ceramics, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for 5 STRAIGHT SCISSORS?

The FDA product code for 5 STRAIGHT SCISSORS is EKJ.

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 American Medical Ceramics, Inc. 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.

View all 11 devices →

Related Devices (Code: EKJ)

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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