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FDA 510(k)

NEEDLES AND SUTURES, SILK & NYLON

K-Number: K760158 · 1976-08-19

ApplicantAlcon Laboratories
Decision Date1976-08-19
Product CodeGAP
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

NEEDLES AND SUTURES, SILK & NYLON is the device name listed in this FDA 510(k) record. The listed applicant is Alcon Laboratories. It received FDA 510(k) clearance on 1976-08-19 under 510(k) number K760158. The device is classified under product code GAP. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEEDLES AND SUTURES, SILK & NYLON?

NEEDLES AND SUTURES, SILK & NYLON is a medical device that received FDA 510(k) clearance on 1976-08-19. The listed applicant is Alcon Laboratories. The 510(k) number is K760158.

When did NEEDLES AND SUTURES, SILK & NYLON receive FDA 510(k) clearance?

NEEDLES AND SUTURES, SILK & NYLON received FDA 510(k) clearance on 1976-08-19, under 510(k) number K760158.

Who is the listed applicant for NEEDLES AND SUTURES, SILK & NYLON?

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

What is the FDA product code for NEEDLES AND SUTURES, SILK & NYLON?

The FDA product code for NEEDLES AND SUTURES, SILK & NYLON is GAP.

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Other records listing Alcon Laboratories 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.

K062624NEXT GENERATION LASERK062865SMALL VOLUME SYRINGEK000148RGP MULTI-PURPOSE SOLUTION ID 100136K984573OPTI-FREE EXPRESS MULTI-ACTION CLEANING AND REWETTING DROPK990480OPTI-FREE SUPRACLENS DAILY PROTEIN REMOVERK984575MULTI-PURPOSE DISINFECTING SOLUTION ID 90746

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Related Devices (Code: GAP)

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.

K241486Sofsilk™ Coated Braided Silk SutureCovidienK222944SafePath Sulturing System-Silk Suture, SafePath Sulturing System Polyamide Suture (Nylon) SafePath Sulturing System- Polypropylene SutureSafepath Medical, Inc.K232355Non absorbable Surgical Silk SutureShandong Haidike Medical Product Co., Ltd.K221767Surgical Sutures with or without NeedleHuaian Seamen Medical Technology Co., Ltd.K180701SafePath Suturing SystemSafepath Medical, Inc.K172149FILASILK - Natural Non-absorbable Silk Surgical Suture, FILAMIDE - Non Absorbable polyamide surgical Sutures, MERICRON XL - Non Absorbable Polyester Surgical Suture, FILAPROP - Non Absorbable Polypropylene surgical SutureM/s. Meril Endo Surgery Private Limited.

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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