HK Aspirator Pump 230 V AP-230III

GUDID 08169890200166

HK Aspirator Pump 230 V

HK SURGICAL INC.

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Primary Device ID08169890200166
NIH Device Record Key41054c61-7c47-4428-9107-5ad40474c2b7
Commercial Distribution Discontinuation2020-08-10
Commercial Distribution StatusNot in Commercial Distribution
Brand NameHK Aspirator Pump 230 V
Version Model NumberAP-230III
Catalog NumberAP-230III
Company DUNS106885259
Company NameHK SURGICAL INC.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchfalse
Serial Numbertrue
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Customer Support Contacts

Phone949-369-0101
Emailhkinfo@hksurgical.com
Phone949-369-0101
Emailhkinfo@hksurgical.com
Phone949-369-0101
Emailhkinfo@hksurgical.com
Phone949-369-0101
Emailhkinfo@hksurgical.com
Phone949-369-0101
Emailhkinfo@hksurgical.com
Phone949-369-0101
Emailhkinfo@hksurgical.com
Phone949-369-0101
Emailhkinfo@hksurgical.com
Phone949-369-0101
Emailhkinfo@hksurgical.com
Phone949-369-0101
Emailhkinfo@hksurgical.com
Phone949-369-0101
Emailhkinfo@hksurgical.com
Phone949-369-0101
Emailhkinfo@hksurgical.com
Phone949-369-0101
Emailhkinfo@hksurgical.com
Phone949-369-0101
Emailhkinfo@hksurgical.com
Phone949-369-0101
Emailhkinfo@hksurgical.com

Device Identifiers

Device Issuing AgencyDevice ID
GS108169890200166 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

MUUSystem, Suction, Lipoplasty

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2020-08-11
Device Publish Date2016-09-21

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