Atlas FDA

GOMCO CIRCUMCISION CLAMP, MOGEN CLAMP, PLASTIBELL CIRCUMCISION DEVICE

FDA 510(k) clearance K061539 · decided 2007-09-20

Clearance details

K-number
K061539
Device name
GOMCO CIRCUMCISION CLAMP, MOGEN CLAMP, PLASTIBELL CIRCUMCISION DEVICE
Applicant
Clinical Innovations, LLC
Decision
Substantially Equivalent
Date received
2006-06-05
Decision date
2007-09-20
Days to decision
472 days
Clearance type
Traditional
Product code
HFX
Device class
2
Regulation number
884.4530
Medical specialty
Obstetrics/Gynecology
Advisory committee
Obstetrics/Gynecology
Location
Murray, UT, US
Third-party review
No
Expedited review
No

+ Add to Predicate Builder ◉ Watch Clinical Innovations

Need this as data, not a web page?

Query all 176,000+ clearances through the Atlas FDA API, or subscribe to weekly change alerts. Self-serve from $29/mo.

Similar devices under this product code

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

RecordFirmDate
Konig Bell Circumcision Clamp (K251687)Medline Industries, LP2026-02-25
Wee Bell (K221356)Wee Medical2023-02-02
Konig Mogen Clamp (K212911)Medline Industries, Inc.2022-11-18
Circumplast Circumcision Device (K151095)Novadien Healthcare2015-09-18
MALE CIRCUMCISION KITS:RAPIDECLAMP (K142163)Medicfit Technology Sdn Bhd2015-04-20
SHANGRING (K131373)Wuhu Snnda Medical Treatment Appliance Technology2013-06-25
SHANGRING (K121789)Wuhu Snna Medical Treatment Appliance Technology C2012-08-03
PREPEX SYSTEM (K103695)Circ Medtech2012-01-10
MEDICON MOGEN CLAMP (K100916)Medicon EG2010-12-06
GMD UNIVERSAL CIRCUMCISION CLAMP, MODEL 200 (K063429)Generic Medical Device, Inc.2007-01-17
SURGICAL DESIGN CIRCUMCISION CLAMP (K043533)Surgical Design, Inc.2005-04-01
FINE SURGICAL CIRCUMCISION CLAMP (K040052)Fine Surgical Instrument Corp.2004-04-09

Recalls involving this device

No recalls on record reference this clearance.