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FDA 510(k)

STEPHENS DISPOSABLE SCISSORS

K-Number: K022840 · 2002-11-01

ApplicantStephens Instruments
Decision Date2002-11-01
Product CodeHNF
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

STEPHENS DISPOSABLE SCISSORS is the device name listed in this FDA 510(k) record. The listed applicant is Stephens Instruments. It received FDA 510(k) clearance on 2002-11-01 under 510(k) number K022840. The device is classified under product code HNF. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STEPHENS DISPOSABLE SCISSORS?

STEPHENS DISPOSABLE SCISSORS is a medical device that received FDA 510(k) clearance on 2002-11-01. The listed applicant is Stephens Instruments. The 510(k) number is K022840.

When did STEPHENS DISPOSABLE SCISSORS receive FDA 510(k) clearance?

STEPHENS DISPOSABLE SCISSORS received FDA 510(k) clearance on 2002-11-01, under 510(k) number K022840.

Who is the listed applicant for STEPHENS DISPOSABLE SCISSORS?

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

What is the FDA product code for STEPHENS DISPOSABLE SCISSORS?

The FDA product code for STEPHENS DISPOSABLE SCISSORS is HNF.

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.

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Other records listing Stephens Instruments 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.

K022836STEPHENS DISPOSABLE SPECULUMK022835STEPHENS DISPOSABLE FORCEPSK022842STEPHENS DISPOSABLE HOOKSK022843GAYHEART CORNEAL EXCISION DEVICE

Related Devices (Code: HNF)

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.

K897093INTRAOCULAR MICROSCISSORS BY MEANS OF GAMMA RADIA.Microline Pentax, Inc.K873099MANUAL OPHTHALMIC SURGICAL INSTRUMENTSAlcon LaboratoriesK85176813-550,13-560 WESCOTT SCOSSORS (EYE)ArtiberiaK822151SURGICAL INSTRUMENTS REPRESENT. 4 CLASSRobert I. Chien & Assoc., Inc.K821290LITTAUER SCISSORS 5 1/2Conphar, Inc.K821286IRIS SCISSORS STRAIGHT 4 1/2Conphar, Inc.

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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