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)

ULTRASAFE ASPIRATING SYRINGE

K-Number: K944425 · 1995-01-26

ApplicantSafety Syringes, Inc.
Decision Date1995-01-26
Product CodeMEG
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ULTRASAFE ASPIRATING SYRINGE is the device name listed in this FDA 510(k) record. The listed applicant is Safety Syringes, Inc.. It received FDA 510(k) clearance on 1995-01-26 under 510(k) number K944425. The device is classified under product code MEG. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ULTRASAFE ASPIRATING SYRINGE?

ULTRASAFE ASPIRATING SYRINGE is a medical device that received FDA 510(k) clearance on 1995-01-26. The listed applicant is Safety Syringes, Inc.. The 510(k) number is K944425.

When did ULTRASAFE ASPIRATING SYRINGE receive FDA 510(k) clearance?

ULTRASAFE ASPIRATING SYRINGE received FDA 510(k) clearance on 1995-01-26, under 510(k) number K944425.

Who is the listed applicant for ULTRASAFE ASPIRATING SYRINGE?

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

What is the FDA product code for ULTRASAFE ASPIRATING SYRINGE?

The FDA product code for ULTRASAFE ASPIRATING SYRINGE is MEG.

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 Safety Syringes, 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.

K123743ULTRASAFE PLUS PASSIVE NEEDLE GUARDK122558ULTRASAFE PASSIVE NEEDLE GUARDK060743MODIFICATION TO: TAMPER EVIDENT ULTRASAFE PASSIVE DELIVERY SYSTEM, ULTRASAFE PASSIVE DELIVERY SYSTEM (X-SERIES)K042712TAMPER EVIDENT ULTRASAFE PASSIVE DELIVERY SYSTEMK013801ULTRASAFE DENTAL INJECTION SYSTEMK011369ULTRASAFE PASSIVE X-SERIES, NEEDLE GUARD SYRINGE, PISTON (ACCESSORY)

View all 10 devices →

Related Devices (Code: MEG)

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.

K252098PA3X Detachable Safety Sleeve Syringe (with needle) (SC-23ED / SD-23ED)Methyl Co., Ltd.K250847VaporShieldVault Paragon Group, Inc.K230287SaviSafe Safety DeviceSuzhou Savicred Biotechnology Co., Ltd.K231165Shina Syringe; Shina Safety SyringeShina Med CorporationK231907Medline Safety Insulin and TB SyringesMedline Industries, LPK223376Monoject Magellan Insulin Safety Syringe 1mL, 31G x 6mm (8881893110); Monoject Magellan Insulin Safety Syringe 0.5mL, 31G x 6mm (8881893150); Monoject Magellan Insulin Safety Syringe 0.3mL, 31G x 6mm (8881893130)Cardinal Health200, LLC

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.

↑