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FDA 510(k)

ALL-VUE ULTRA-LITE THIN WALL SYRINGE SHIELD

K-Number: K934549 · 1994-02-19

ApplicantVictoreen, Inc.
Decision Date1994-02-19
Product CodeIWR
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ALL-VUE ULTRA-LITE THIN WALL SYRINGE SHIELD is the device name listed in this FDA 510(k) record. The listed applicant is Victoreen, Inc.. It received FDA 510(k) clearance on 1994-02-19 under 510(k) number K934549. The device is classified under product code IWR. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ALL-VUE ULTRA-LITE THIN WALL SYRINGE SHIELD?

ALL-VUE ULTRA-LITE THIN WALL SYRINGE SHIELD is a medical device that received FDA 510(k) clearance on 1994-02-19. The listed applicant is Victoreen, Inc.. The 510(k) number is K934549.

When did ALL-VUE ULTRA-LITE THIN WALL SYRINGE SHIELD receive FDA 510(k) clearance?

ALL-VUE ULTRA-LITE THIN WALL SYRINGE SHIELD received FDA 510(k) clearance on 1994-02-19, under 510(k) number K934549.

Who is the listed applicant for ALL-VUE ULTRA-LITE THIN WALL SYRINGE SHIELD?

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

What is the FDA product code for ALL-VUE ULTRA-LITE THIN WALL SYRINGE SHIELD?

The FDA product code for ALL-VUE ULTRA-LITE THIN WALL SYRINGE SHIELD is IWR.

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Other records listing Victoreen, 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.

K982937MODEL 580-006 RADIATION THERAPY IONIZATION CHAMBERK974112VACUDAP, MODEL 2000, 2001K973960MODEL 37-185K964952VERIDOSE V (FIVE), MODEL NUMBER 37-705K964785VERIDOSE DIODESK971382PRONE BREAST POSITIONING BOARD, MODEL #37-018

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Related Devices (Code: IWR)

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.

K872656LEAD GLASS SHIELDSViox Corp.K863936DUFFY BOLUS INJECTORViox Corp.K811688TUNGSTEN SYRINGE SHIELDMedi-Physics Inc. Dba Nycomed Amersham Imaging

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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