Medical Device Manufacturer · US , Norcross , GA

Ssl Americas, Inc. - FDA 510(k) Cleared Devices

10 submissions · 10 cleared · Since 2002

Total

Cleared

Denied

Ssl Americas, Inc. has 10 FDA 510(k) cleared obstetrics & gynecology devices. Based in Norcross, US.

Historical record: 10 cleared submissions from 2002 to 2008.

Browse the complete list of FDA 510(k) cleared obstetrics & gynecology devices from this manufacturer. Filter by specialty or product code using the sidebar.

Ssl Americas, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Ssl Americas, Inc.

10 devices

1-10 of 10

Cleared Jun 19, 2008

DUREX SYNTHETIC POLYISOPRENE MALE CONDOM

K072169 · MOL

Obstetrics & Gynecology · 318d

Cleared Mar 10, 2008

DUREX PLAY MASSAGE GEL LUBRICANT

K063385 · NUC

Obstetrics & Gynecology · 488d

Cleared Jun 08, 2006

DUREX PLAY TEMPTATIONS ASSORTED LUBRICANTS

K060098 · NUC

Obstetrics & Gynecology · 146d

Cleared Apr 08, 2005

DUREX PLAY TINGLING LUBRICANT

K042958 · NUC

Obstetrics & Gynecology · 163d

Cleared Apr 05, 2005

DUREX SPEARMINT SCENTED LUBRICATED LATEX CONDOM (DUREX 'TINGLING PLEASURE'...

K042470 · HIS

Obstetrics & Gynecology · 204d

Cleared Feb 23, 2005

DUREX PLAY WARMER LUBRICANT

K042563 · KMJ

General Hospital · 155d

Cleared Mar 29, 2004

DUREX FLAVORED LATEX CONDOM

K032227 · HIS

Obstetrics & Gynecology · 252d

Cleared Mar 11, 2004

FLIGHT SOCK

K040353 · DWL

General Hospital · 28d

Cleared Jan 16, 2004

DUREX PLAY LUBRICANT

K032124 · HIS

Obstetrics & Gynecology · 190d

Cleared Mar 29, 2002

DUREX LATEX CONDOM WITH MALE GENITAL DESENSITIZER LUBRICANT

K020659 · HIS

Obstetrics & Gynecology · 28d

Ssl Americas, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Ssl Americas, Inc.

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