FDA 510(k) FDA class 2 Substantially Equivalent 🇹🇼 Taiwan

AbClose - Port Site Closure Device

K Number: K193652 · Decision Mar 26, 2020
Classifications
1
FEI Numbers
52
Registration Numbers
52
Same Product Code
69
Applicant Total
7
Review Days
87

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Basic Information

Device Name
AbClose - Port Site Closure Device
K Number
K193652
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1500
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Medeon Biodesign, Inc.
Date Received
December 30, 2019
Decision Date
March 26, 2020
Product Code
OCW
Advisory Committee
Gastroenterology, Urology
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
OCW Endoscopic Tissue Approximation Device

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (OCW), ordered by most recent decision date.

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Other Clearances by Medeon Biodesign, Inc.

K Number Device Name
K200902 ClickClean
K192891 Laparoscope Lens Shield Device (LENS)
K170103 Laparoscope Lens Shield Device (LENS)
K160117 AbClose - Port Site Closure Device
K160172 Laparoscope Lens Shield Device
K151117 Laparoscope Lens Shield Device