FDA 510(k)

TRANSIGEN EXUDATE CONTROLLED WOUND DRESSING

K-Number: K872988 · 1987-09-16

Decision Date1987-09-16

Product CodeNAD

Advisory CommitteeSU

DecisionSubstantially Equivalent for Some Indications

Device Summary

TRANSIGEN EXUDATE CONTROLLED WOUND DRESSING 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 1987-09-16 under 510(k) number K872988. The device is classified under product code NAD. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the TRANSIGEN EXUDATE CONTROLLED WOUND DRESSING?

TRANSIGEN EXUDATE CONTROLLED WOUND DRESSING is a medical device that received FDA 510(k) clearance on 1987-09-16. The listed applicant is Smith & Nephew, Inc.. The 510(k) number is K872988.

When did TRANSIGEN EXUDATE CONTROLLED WOUND DRESSING receive FDA 510(k) clearance?

TRANSIGEN EXUDATE CONTROLLED WOUND DRESSING received FDA 510(k) clearance on 1987-09-16, under 510(k) number K872988.

Who is the listed applicant for TRANSIGEN EXUDATE CONTROLLED WOUND DRESSING?

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 TRANSIGEN EXUDATE CONTROLLED WOUND DRESSING?

The FDA product code for TRANSIGEN EXUDATE CONTROLLED WOUND DRESSING is NAD.

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_RECRUITING NCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITING NCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDED NCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Smith & Nephew, Inc. as applicant

K261462LANDMARK Total Knee System K261968Q-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 Glenoids K252416AETOS Shoulder System Meta Humeral Prosthesis Size 0 K252129AETOS Shoulder System Stemless Humeral Prosthesis K251627BIORAPTOR 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: NAD)

K254246LT Antibacterial Foam with Silver DressingZhejiang Longterm Medical Technology Co., Ltd.K102403SAM CHEST SEAL WITH VAVLE; SAM CHEST SEALSam Medical Products K091133APLION TOPICAL CARE SYSTEMAplion Medical,Llc K072560ENVELA (HYDROHESIVE OCCLUSIVE DRESSING)Teikoku Pharma USA, Inc.K080524CENTURION SORBAVIEW OTCTri-State Hospital Supply Corp.K060046DERMASTREAMEnzysurge , Ltd.

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.