FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

Relizorb

K Number: K163057 · Decision Jul 12, 2017
Classifications
1
FEI Numbers
2
Registration Numbers
2
Same Product Code
7
Applicant Total
7
Review Days
253

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Basic Information

Device Name
Relizorb
K Number
K163057
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5985
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Alcresta Therapeutics, Inc.
Date Received
November 1, 2016
Decision Date
July 12, 2017
Product Code
PLQ
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

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

Product Code Device Name
PLQ Enzyme Packed Cartridge

Similar 510(k) Clearances

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

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Other Clearances by Alcresta Therapeutics, Inc.

K Number Device Name
K250499 RELiZORB (100300/100301)
K243284 RELiZORB (100300/ 100301)
K232784 RELiZORB®
K231156 Enzyme Packed Cartridge - RELiZORB
K191379 RELiZORB
K161247 Relizorb