Medical Device Manufacturer · US , Mchenry , IL

Wien Laboratories, Inc. - FDA 510(k) Cleared Devices

13 submissions · 13 cleared · Since 1977

Total

Cleared

Denied

Wien Laboratories, Inc. has 13 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 13 cleared submissions from 1977 to 1991. Primary specialty: Chemistry.

Browse the FDA 510(k) cleared devices submitted by Wien Laboratories, Inc. Filter by specialty or product code using the sidebar.

Wien Laboratories, 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 - Wien Laboratories, Inc.

13 devices

1-12 of 13

PROGESTERONE TEST SET 125I 17-OH

K834246 · JLX

Chemistry · 59d

Cleared Sep 12, 1983

ANDROSTENEDIONE TEST SET 125I

K832452 · CIZ

Chemistry · 49d

Cleared Nov 29, 1982

125 I-DEHYDROEPIANDROSTERONE SULFATE

K823200 · JKC

Chemistry · 34d

Cleared Jun 14, 1982

DOXEPIN TRI-CY TEST SET

K821652 · LFG

Chemistry · 11d

Cleared Jun 14, 1982

PROTRIPTYLINE TRI-CY TEST SET

K821653 · LFG

Chemistry · 11d

Cleared Dec 11, 1980

125I-TESTOSTERONE TEST SET

K802728 · CDZ

Chemistry · 38d

Cleared Oct 30, 1979

DHEA-SULFATE TEST SET

K792041 · JKC

Chemistry · 18d

Cleared Jan 03, 1979

TEST SET, 125 I-DIGOXIN

125I DIGOXIN TEST SET

Wien Laboratories, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Wien Laboratories, Inc.

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