Medical Device Manufacturer · US , Mchenry , IL

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

19 submissions · 19 cleared · Since 1981

Total

Cleared

Denied

Bio-Analytics Laboratories, Inc. has 19 FDA 510(k) cleared chemistry devices. Based in Mchenry, US.

Historical record: 19 cleared submissions from 1981 to 1986.

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

Bio-Analytics 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 - Bio-Analytics Laboratories, Inc.

19 devices

1-19 of 19

Cleared May 29, 1986

KINETIC ALKALINE PHOSPHATASE REAGENT KIT

K861638 · CJE

Chemistry · 29d

Cleared Mar 14, 1986

ENZYMATIC ALPHA-AMYLASE REAGENT KIT

ULTRA-VIOLET BUN REAGENT KIT

K851513 · CDQ

Chemistry · 35d

Cleared May 20, 1985

ULTRA-VIOLET GLUCOSE REAGENT

K851514 · CFA

Chemistry · 35d

Cleared Mar 05, 1985

ENZYMATIC ALPHA-AMYLASE REAGENT KIT

ACETAMINOPHEN(PARACETAMOL

BIO-CAL OPERATION CHECK KIT

UREA NITROGEN, KINETIC

K810087 · JGZ

Chemistry · 44d

Cleared Jan 28, 1981

LDH-L LIQUID ENZYMATIC, KINETIC KIT

URIC ACID (TPTZ) COLORINMETRIC

K810088 · CDH

Chemistry · 15d

Cleared Jan 26, 1981

ALKALINE PHOSPH., LIQUID ENZY., KIN. KIT

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

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

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