Atlas FDA

COOPERSURGICAL LAPAROSCOPIC INSTRUMENTS

FDA 510(k) clearance K021237 · decided 2003-04-10

Clearance details

K-number
K021237
Device name
COOPERSURGICAL LAPAROSCOPIC INSTRUMENTS
Applicant
CooperSurgical, Inc.
Decision
Substantially Equivalent
Date received
2002-04-18
Decision date
2003-04-10
Days to decision
357 days
Clearance type
Traditional
Product code
HET
Device class
2
Regulation number
884.1720
Medical specialty
Obstetrics/Gynecology
Advisory committee
Obstetrics/Gynecology
Location
Tuningen, DE
Third-party review
No
Expedited review
No

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Devices cleared under the same product code - the starting set for predicate research.

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Recalls involving this device

No recalls on record reference this clearance.

PMA approvals by this applicant

RecordFirmDate
Mara Water Vapor Ablation System (P160047/S039)CooperSurgical, Inc.2025-01-07
MARA Water Vapor Ablation System (P160047/S035)CooperSurgical, Inc.2024-07-11
MARA Water Vapor Ablation System (P160047/S038)CooperSurgical, Inc.2024-07-09
MARA Water Vapor Ablation System (P160047/S036)CooperSurgical, Inc.2024-05-10
Mater Water Vapor System - Model # GEA-SYS-16-0500, Mara Water Vapor Probe Kit - Model # DDK-16-050, Mara Console - Mode (P160047/S034)CooperSurgical, Inc.2023-12-08
MARA Water Vapor Ablation System (P160047/S033)CooperSurgical, Inc.2023-10-25
Mara Water Vapor Ablation System (P160047/S031)CooperSurgical, Inc.2023-07-28
Mara Water Vapor Ablation System (P160047/S032)CooperSurgical, Inc.2023-07-27