FDA 510(k) FDA class 2 Unknown 🇺🇸 United States

GASTRIC PORT, MODELS: GAP-0016-00, GAP-0018-00, GAP-0020-00

K Number: K082102 · Decision Jun 14, 2010
Classifications
1
FEI Numbers
116
Registration Numbers
116
Same Product Code
100
Applicant Total
12
Review Days
689

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Basic Information

Device Name
GASTRIC PORT, MODELS: GAP-0016-00, GAP-0018-00, GAP-0020-00
K Number
K082102
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1500
Medical Specialty
Gastroenterology, Urology
Decision
Unknown
Statement or Summary
Summary
Applicant
Apollo Endosurgery, Inc.
Date Received
July 25, 2008
Decision Date
June 14, 2010
Product Code
FED
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
FED Endoscopic Access Overtube, Gastroenterology-Urology

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Other Clearances by Apollo Endosurgery, Inc.

K Number Device Name
K232544 Apollo ESG NXT System, Apollo REVISE NXT System
K231553 OverStitch NXT Endoscopic Suturing System
DEN210045 APOLLO ESG System, APOLLO ESG SX System, APOLLO REVISE System, APOLLO REVISE SX System
K210266 OverStitch Sx Endoscopic Suturing System
K201808 X-Tack Endoscopic HeliX Tacking System
K171886 OverStitch SX Endoscopic Suturing System (ESS)
K122270 OVERTUBE ENDOSCOPIC ACCESS SYSTEM
K103155 SUMO ACCESS AND TISSUE RESECTION SYSTEM
K090583 ENDOSCOPIC MONOPOLAR SCISSORS, MODELS EMS-235, EMS-165
K082114 ELECTROCAUTERY DILATION BALLOON, MODELS: EDB-0018-00, EDB-0020-00, EDB-0022-00
Search all 12 clearances from Apollo Endosurgery, Inc. →