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

APOLLO ESG System, APOLLO ESG SX System, APOLLO REVISE System, APOLLO REVISE SX System

K Number: DEN210045 · Decision Jul 12, 2022
Classifications
1
FEI Numbers
6
Registration Numbers
6
Same Product Code
1
Applicant Total
12
Review Days
285

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Basic Information

Device Name
APOLLO ESG System, APOLLO ESG SX System, APOLLO REVISE System, APOLLO REVISE SX System
K Number
DEN210045
Device Class
FDA class 2
Clearance Type
Direct
Regulation Number
876.5983
Medical Specialty
Gastroenterology, Urology
Decision
Unknown
Applicant
Apollo Endosurgery, Inc.
Date Received
September 30, 2021
Decision Date
July 12, 2022
Product Code
QTD
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
QTD Endoscopic Suturing Device For Altering Gastric Anatomy For Weight Loss

Similar 510(k) Clearances

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

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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
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
K082102 GASTRIC PORT, MODELS: GAP-0016-00, GAP-0018-00, GAP-0020-00
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. →