Atlas FDA

VAS DILATOR

FDA 510(k) clearance K922192 · decided 1992-08-07

Clearance details

K-number
K922192
Device name
VAS DILATOR
Applicant
Cook Urological, Inc.
Decision
Substantially Equivalent
Date received
1992-05-11
Decision date
1992-08-07
Days to decision
88 days
Clearance type
Traditional
Product code
KOA
Device class
1
Regulation number
876.4730
Medical specialty
Gastroenterology, Urology
Advisory committee
Gastroenterology, Urology
Location
Spencer, IN, US
Third-party review
No
Expedited review
No

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RecordFirmDate
FiXcision (K182664)Agency For Medical Innovations GmbH2018-12-07
URETHRAL SUTURE GUIDE (K950267)Applied Medical Resources1995-01-31
LI VASECTOMY (K932465)Femcare , Ltd.1994-03-02
VASOVASOSTOMY SET (K921546)Cook Urological, Inc.1993-07-02
VESITEC SUTURE PASSER (K931181)Vesitec Medical, Inc.1993-05-12
DDV LIGATOR (K921304)North American Medical, Inc.1992-10-05
NO-SCALPEL VASCETOMY INSTRUMENTS (K922971)Pilling Co.1992-09-23
BENDEREV PROTECT-A-PASS NEEDLE (K921228)Eimark Labs, Inc.1992-09-14
GRASPING FORCEPS (K896058)Annex Medical, Inc.1989-12-28
MARLOW ANAL SPECULUM (K891352)Simpson/Basye, Inc.1989-06-23
MICROSURGICAL CYSTOTOME (K890218)Kinetic Medical Products1989-01-27
STOMACH EVACULATOR - EWALD STYLE (K864963)Medovations, Inc.1987-10-14

Recalls involving this device

No recalls on record reference this clearance.