FDA 510(k)

PRO-TIP DISPOSABLE 3/1 SYRINGE NOZZLE

K-Number: K923285 · 1992-09-15

Decision Date1992-09-15

Product CodeECB

Advisory CommitteeDE

DecisionSubstantially Equivalent

Device Summary

PRO-TIP DISPOSABLE 3/1 SYRINGE NOZZLE 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 1992-09-15 under 510(k) number K923285. The device is classified under product code ECB. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PRO-TIP DISPOSABLE 3/1 SYRINGE NOZZLE?

PRO-TIP DISPOSABLE 3/1 SYRINGE NOZZLE is a medical device that received FDA 510(k) clearance on 1992-09-15. The listed applicant is Smith & Nephew, Inc.. The 510(k) number is K923285.

When did PRO-TIP DISPOSABLE 3/1 SYRINGE NOZZLE receive FDA 510(k) clearance?

PRO-TIP DISPOSABLE 3/1 SYRINGE NOZZLE received FDA 510(k) clearance on 1992-09-15, under 510(k) number K923285.

Who is the listed applicant for PRO-TIP DISPOSABLE 3/1 SYRINGE NOZZLE?

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 PRO-TIP DISPOSABLE 3/1 SYRINGE NOZZLE?

The FDA product code for PRO-TIP DISPOSABLE 3/1 SYRINGE NOZZLE is ECB.

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: ECB)

K942519UNI-SYRINGE, UNI-TIP AND ACCESS SYRINGE TIPSBull Frog Mfg. Co.K931772SURETIP SYRINGE TIP COVERWestern M/D, Inc.K931137DENTAL SYRINGE TIPA-Dec, Inc.K923876RISKONTROL SINGLE USERiskontrol K920499SANI-TIPDw Industries, Inc.K911756POSTERIOR NASAL EPISTAXIS INSTRUMENTSRichard Wolf Medical Instruments Corp.

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.