Atlas FDA

ATRAUMATIC TENACULA

FDA 510(k) clearance K930037 · decided 1994-02-24

Clearance details

K-number
K930037
Device name
ATRAUMATIC TENACULA
Applicant
Thomasville Medical Assoc.
Decision
Substantially Equivalent
Date received
1993-01-05
Decision date
1994-02-24
Days to decision
415 days
Clearance type
Traditional
Product code
HDC
Device class
2
Regulation number
884.4530
Medical specialty
Obstetrics/Gynecology
Advisory committee
Obstetrics/Gynecology
Location
Alpharetta, GA, 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
Carevix™ Suction Cervical Stabilizer (K223866)Aspivix SA2023-01-25
ASPIVIX v1.1 Cervical Suction Tenaculum (K203820)Aspivix SA2021-08-17
Bioceptive Suction Cervical Retractor (K142204)Bioceptive, Inc.2014-12-19
JARIT HULKA UTERINE TENACULUM FORCEPS (K082349)J. Jamner Surgical Instruments, Inc.2008-11-21
GYN DISPOSABLES TENACULUM 356T (K073182)Gyn-Disposables, Inc.2007-11-28
FEMTEN CERVICAL TENACULUM (K062563)Fem Suite, LLC2007-05-18
BURBANK TENACULUM (K060573)Vascular Control Systems, Inc.2006-04-21
TRANSVAGINAL ULTRASOUND PROBE HOLDER SYSTEM (K032585)Ron-Tech Medical , Ltd.2004-01-09
BURBANK TENACULUM, MODEL 09-0011-01 (K030078)Vascular Control Systems, Inc.2003-01-24
UTERINE TENACLUM HOOK (K001818)Towne Brothers (Pvt.), Ltd.2000-08-30
TRANSVAGINAL ULTRASOUND PROBE HOLDER DEVICE (K992071)Ron-Tech Medical , Ltd.1999-08-27
GYNEX IRIS HOOK, GYNEX ANGLE HOOK, GYNEX EMMETT TENACULUM (K980247)Gynex Corp.1998-03-17

Recalls involving this device

No recalls on record reference this clearance.