Schmid Laboratories, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Schmid Laboratories, Inc. - FDA 510(k) Cleared Devices
10
Total
9
Cleared
0
Denied
Schmid Laboratories, Inc. has 9 FDA 510(k) cleared obstetrics & gynecology devices. Based in Mchenry, US.
Historical record: 9 cleared submissions from 1980 to 1990.
Browse the complete list of FDA 510(k) cleared obstetrics & gynecology devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Schmid Laboratories, Inc.
10 devices
Cleared
Jul 13, 1990
THIN CONDOM RAMSES & SHEIK
Obstetrics & Gynecology
198d
Cleared
Jun 07, 1990
MINT SCENTED CONDOMS
Obstetrics & Gynecology
115d
Cleared
Mar 01, 1989
STANDARD LATEX CONDOM
Obstetrics & Gynecology
133d
Cleared
Oct 26, 1988
CONDOMS (RAMSES, SHEIK AND KOROMEX)
Obstetrics & Gynecology
107d
Cleared
Jun 21, 1988
OKAMOTO CONDOMS SPERMICIDALLY LUBRICATED
Obstetrics & Gynecology
112d
Cleared
Apr 12, 1988
CONDOMS (RAMSES EXTRA, SHEIK ELITE AND KOROMEX)
Obstetrics & Gynecology
141d
Cleared
Feb 26, 1988
OKAMOTO CONDOMS
Obstetrics & Gynecology
38d
Cleared
Dec 08, 1987
STANDARD LATEX CONDOMS (RAMSES, SHEIK AND KOROMEX)
Obstetrics & Gynecology
21d
Cleared
Nov 03, 1982
MALE CONDOM
Obstetrics & Gynecology
113d
Cleared
Sep 25, 1980
PROPHYLACTIC W/SPERMICIDAL LUBRICANT
Obstetrics & Gynecology