Atlas FDA

COLPOSCOPE SYSTEM

FDA 510(k) clearance K770697 · decided 1977-05-20

Clearance details

K-number
K770697
Device name
COLPOSCOPE SYSTEM
Applicant
Richard Wolf Medical Instruments Corp.
Decision
Substantially Equivalent
Date received
1977-04-15
Decision date
1977-05-20
Days to decision
35 days
Clearance type
Traditional
Product code
HEX
Device class
2
Regulation number
884.1630
Medical specialty
Obstetrics/Gynecology
Advisory committee
Obstetrics/Gynecology
Location
Mchenry, IL, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

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

RecordFirmDate
Smart Scope® CX (K233043)Periwinkle Technologies Pvt., Ltd.2024-06-14
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Pocket Colposcope System (K181034)Hadleigh Health Technologies, LLC2018-09-21
LT-300 SD Digital Video Colposcope (K170446)Lutech Industries, Inc.2017-05-21
EVA (Enhanced Visual Assessment) System (K161871)Mobileodt , Ltd.2016-12-19
Colposcope System (K160341)Xuzhou Kernel Medical Equipment Co., Ltd.2016-09-14
LT-300 HD (K160380)Lutech Industries, Inc.2016-05-13
Video Colposcope (K151878)Edan Instruments, Inc.2015-12-01
LT-300 Video Colposcope (K143119)Lutech Industries, Inc.2014-12-18
COOPER SURGICAL LEISEGANG COLPOSCOPE SYSTEM (K140754)CooperSurgical, Inc.2014-10-23
THE GYNOCULAR (K132423)Gynius AB2014-04-08

Recalls involving this device

No recalls on record reference this clearance.

PMA approvals by this applicant

RecordFirmDate
HULKA CLIP FOR TUBAL OCCLUSION (P870080/S002)Richard Wolf Medical Instruments Corp.2016-10-14
HULKA CLIP FOR TUBAL OCCLUSION (P870080/S001)Richard Wolf Medical Instruments Corp.1998-03-12
HULKA CLIP FOR TUBAL OCCLUSION (P870080)Richard Wolf Medical Instruments Corp.1996-09-05
RICHARD WOLF PIEZOLITH E.L.P. LITHOTRIPT MODEL2300 (P890013)Richard Wolf Medical Instruments Corp.1991-09-09