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FDA 510(k)

STEPHENS DISPOSABLE FORCEPS

K-Number: K022835 · 2002-11-01

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

Device Summary

STEPHENS DISPOSABLE FORCEPS 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 K022835. The device is classified under product code HNR. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STEPHENS DISPOSABLE FORCEPS?

STEPHENS DISPOSABLE FORCEPS 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 K022835.

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

STEPHENS DISPOSABLE FORCEPS received FDA 510(k) clearance on 2002-11-01, under 510(k) number K022835.

Who is the listed applicant for STEPHENS DISPOSABLE FORCEPS?

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 FORCEPS?

The FDA product code for STEPHENS DISPOSABLE FORCEPS is HNR.

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 SPECULUMK022842STEPHENS DISPOSABLE HOOKSK022840STEPHENS DISPOSABLE SCISSORSK022843GAYHEART CORNEAL EXCISION DEVICE

Related Devices (Code: HNR)

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.

K895434ALCON FOLDING FORCEPSAlcon LaboratoriesK891487SOFT LENS FOLDING BLOCKWestern Medical Products, Inc.K893199PHACO-INJECTOR(TM) INTRAOCULAR LENS IMPLANT INSTRAllergan Medical OpticsK885230MCDONALD FOLDING FORCEPSAlcon LaboratoriesK881049BRADBURY INTRAOCULAR RETINAL KIT CAT #200Microline Pentax, Inc.K883197IOL IMPLANTATION FORCEPSD & D Surgical

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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