Procedure Products Syringes

GUDID B1604920Y1

10cc Syringe, Yellow palm-pad plunger

PROCEDURE PRODUCTS, INC.

General-purpose syringe, single-use

• Primary Device ID: B1604920Y1
• NIH Device Record Key: cd167042-4488-4353-80e4-8a67b5464504
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Procedure Products Syringes
• Version Model Number: 4920-Y
• Company DUNS: 151507563
• Company Name: PROCEDURE PRODUCTS, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	B1604920Y1 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K884985

FDA Product Code

• FMF: Syringe, Piston

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: true

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-09-12
• Device Publish Date: 2018-04-19

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