FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

AMSINO SUTURE REMOVAL KIT

K Number: K050656 · Decision May 2, 2005
Classifications
1
FEI Numbers
56
Registration Numbers
56
Same Product Code
14
Applicant Total
28
Review Days
49

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Basic Information

Device Name
AMSINO SUTURE REMOVAL KIT
K Number
K050656
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4800
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Amsino International, Inc.
Date Received
March 14, 2005
Decision Date
May 2, 2005
Product Code
MCZ
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
MCZ Suture Removal Kit

Similar 510(k) Clearances

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Other Clearances by Amsino International, Inc.

K Number Device Name
K252543 AMSafe Administration Set (BA-70075, BA-70071-D, BA-70070, BA-70071-P, BA-70072, BA-70072-F, BA-70071-DF, BA-70071-DF-120, FE01, FE04)
K220230 AMSure Enteral Feeding Pump
K220267 AMSafe NeuFlo Needleless Connector
K213522 AMSafe Pre-Filled Normal Saline Flush Syringe
K200051 PUGGLE Enteral Feeding Pump and Feeding Set
K183473 AMSafe(R) Pre-Filled Normal Saline Flush Syringe
K181445 AMSure Hydrophilic Intermittent Catheter
K181423 AMSure Sterile Water, and Sterile Normal Saline for Wound Flush
K173665 AMSafe Sure-Lok Needle-Free Connector
K181814 AMSure Pre-filled Syringe for Balloon Inflation with Sterile Water
Search all 28 clearances from Amsino International, Inc. →