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FDA 510(k)

SHARPOINT ULTRAPLUG EXTENDED WEAR PLUG

K-Number: K020882 · 2002-07-26

ApplicantSurgical Specialties Corp
Decision Date2002-07-26
Product CodeLZU
DecisionSubstantially Equivalent

Device Summary

SHARPOINT ULTRAPLUG EXTENDED WEAR PLUG is the device name listed in this FDA 510(k) record. The listed applicant is Surgical Specialties Corp. It received FDA 510(k) clearance on 2002-07-26 under 510(k) number K020882. The device is classified under product code LZU. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SHARPOINT ULTRAPLUG EXTENDED WEAR PLUG?

SHARPOINT ULTRAPLUG EXTENDED WEAR PLUG is a medical device that received FDA 510(k) clearance on 2002-07-26. The listed applicant is Surgical Specialties Corp. The 510(k) number is K020882.

When did SHARPOINT ULTRAPLUG EXTENDED WEAR PLUG receive FDA 510(k) clearance?

SHARPOINT ULTRAPLUG EXTENDED WEAR PLUG received FDA 510(k) clearance on 2002-07-26, under 510(k) number K020882.

Who is the listed applicant for SHARPOINT ULTRAPLUG EXTENDED WEAR PLUG?

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

What is the FDA product code for SHARPOINT ULTRAPLUG EXTENDED WEAR PLUG?

The FDA product code for SHARPOINT ULTRAPLUG EXTENDED WEAR PLUG is LZU.

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Other records listing Surgical Specialties Corp 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.

K080985QUILL SELF-RETAINING SYSTEM (SRS) COMPRISED OF POLYDIOXANONE (PDO)K080680QUILL SELF-RETAINING SYSTEM (SRS) COMPRISED OF PDO (POLYDIOXANONEK071989QUILL SELF-RETAINING SYSTEM (SRS) SYNTHETIC ABSORBABLE SURGICAL SUTURE MATERIALK072028QUILL SELF-RETAINING SYSTEM (SRS) COMPRISED OF MONODERMK063680SHARPOINT PDO (POLYDIOXANONE) SUTURESK053380CONTOUR THREAD SYNTHETIC ABSORBABLE PDO BARBED SUTURE

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Related Devices (Code: LZU)

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.

K241229Hello,eyes® BIO PlugBio Optics Co., Ltd.K222164Visant Medical Canalicular PlugVisant Medical, Inc.K213988SOFT PLUG Extended Duration 180 Tapered Canalicular PlugOasis Medical, Inc.K190210Tear Pool Dissolvable Punctum PlugsAlphamed, Inc.K162361Soft Plug Extended Duration 180 Canalicular PlugOasis Medical, Inc.K161673LacriPro Punctum PlugLacrimedics, Inc.

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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