PK

GUDID 00886874111055

PK INSTRUMENT CORD, PK/SP GENERATOR

INTUITIVE SURGICAL, INC.

Electrical-only medical device connection cable, reusable Electrical-only medical device connection cable, reusable

• Primary Device ID: 00886874111055
• NIH Device Record Key: 88927fda-bfca-40c4-958f-9aaacdb47620
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PK
• Version Model Number: 400228
• Company DUNS: 938647021
• Company Name: INTUITIVE SURGICAL, 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: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Dimensions

• Length: 10 Feet
• Length: 10 Feet

Device Identifiers

Device Issuing Agency	Device ID
GS1	00886874111055 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K061260

FDA Product Code

• NAY: System,surgical,computer controlled instrument

Sterilization

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

[00886874111055]

Hydrogen Peroxide;Moist Heat or Steam Sterilization

[00886874111055]

Hydrogen Peroxide;Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 8
• Public Version Date: 2020-03-02
• Device Publish Date: 2017-01-23

On-Brand Devices [PK]

• 00886874111062: PK INSTRUMENT CORD, G400 GENERATOR
• 00886874111055: PK INSTRUMENT CORD, PK/SP GENERATOR