Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

SMITH & NEPHEW SUBCUTANEOUS ILLUMINATOR

K-Number: K991323 · 1999-07-06

ApplicantSmith & Nephew, Inc.
Decision Date1999-07-06
Product CodeFFS
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

SMITH & NEPHEW SUBCUTANEOUS ILLUMINATOR is the device name listed in this FDA 510(k) record. The listed applicant is Smith & Nephew, Inc.. It received FDA 510(k) clearance on 1999-07-06 under 510(k) number K991323. The device is classified under product code FFS. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SMITH & NEPHEW SUBCUTANEOUS ILLUMINATOR?

SMITH & NEPHEW SUBCUTANEOUS ILLUMINATOR is a medical device that received FDA 510(k) clearance on 1999-07-06. The listed applicant is Smith & Nephew, Inc.. The 510(k) number is K991323.

When did SMITH & NEPHEW SUBCUTANEOUS ILLUMINATOR receive FDA 510(k) clearance?

SMITH & NEPHEW SUBCUTANEOUS ILLUMINATOR received FDA 510(k) clearance on 1999-07-06, under 510(k) number K991323.

Who is the listed applicant for SMITH & NEPHEW SUBCUTANEOUS ILLUMINATOR?

The FDA 510(k) record lists Smith & Nephew, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SMITH & NEPHEW SUBCUTANEOUS ILLUMINATOR?

The FDA product code for SMITH & NEPHEW SUBCUTANEOUS ILLUMINATOR is FFS.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Smith & Nephew, 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.

K261462LANDMARK Total Knee SystemK261968Q-FIX KNOTLESS All-Suture Anchor, 2.8mm, with one black knotless and one blue MINITAPE suture (72205981); Q-FIX KNOTLESS All-Suture Anchor, 2.8mm, with one blue knotless and one black MINITAPE suture (72205982)K254084AETOS Shoulder System - CONCELOC GlenoidsK252416AETOS Shoulder System Meta Humeral Prosthesis Size 0K252129AETOS Shoulder System Stemless Humeral ProsthesisK251627BIORAPTOR 2.3 PK Suture Anchor w/ ULTRABRAID (#2) Suture (cobraid blue); BIORAPTOR 2.3 PK Suture Anchor w/ ULTRABRAID (#2) Suture (cobraid black); BIORAPTOR 2.3 PK Suture Anchor w/ ULTRABRAID (#2) Suture (white); BIORAPTOR CURVED 2.3 PK Suture Anchor w/ ONE 38 ULTRABRAID (#2) Suture (cobraid black); BIORAPTOR CURVED 2.3 PK Suture Anchor w/ ONE 38 ULTRABRAID (#2) Suture (cobraid blue)

View all 509 devices →

Related Devices (Code: FFS)

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.

K072521COOK FIBER OPTIC BUNDLE AND FLEXOR DEFLECTING ACCESS SHEATHCook Urological, Inc.K061622PS SERIESPhotonic Optische Gerate Gesmbh & CokgK063309TRU-CABLETruphatek International, Ltd.K061025ACCUTECH ENDOLITE PROBEAccutech Medical Technologies, Inc.K023633SOVIS OPTIQUE'S ENDOSCOPIC CABLESovis OptiqueK001698MICRO LINK ENDOSCOPIC FIBER CABLE, MODEL B1-90159Cogent Light Technologies, 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.

↑