Medical Device Manufacturer · US , Walker , MI

Troy Biologicals, Inc. - FDA 510(k) Cleared Devices

12 submissions · 12 cleared · Since 1981

Total

Cleared

Denied

Troy Biologicals, Inc. has 12 FDA 510(k) cleared microbiology devices. Based in Walker, US.

Historical record: 12 cleared submissions from 1981 to 1986.

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

Troy Biologicals, 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 - Troy Biologicals, Inc.

12 devices

1-12 of 12

Cleared Apr 21, 1986

BACTI PLATE (DERMATOLOGY) PRODUCT NO. PS-5000

SABOURAUD DEXTROSE AGAR

HEMOPHILUS QUAD 10 PLATE

K823306 · JSI

Hematology · 40d

Cleared Dec 15, 1982

CAMPYLOBACTER SELECTIVE AGAR

K823307 · JSI

Microbiology · 40d

Cleared Dec 15, 1982

STREPTOCOCCUS SELECTIVE AGAR

K823310 · JSI

Microbiology · 40d

Cleared Dec 15, 1982

COLUMBIA V AGAR W/5% HUMAN BLOOD

K823311 · JSH

Microbiology · 40d

Cleared Dec 03, 1982

MYCAREL AGAR MYCOBROTIC AGAR

K823308 · JSJ

Microbiology · 28d

Cleared Dec 03, 1982

MARTIN & LEMIS AGAR W/VCAT INHIBITOR

K823309 · JTY

Microbiology · 28d

Cleared Feb 05, 1981

DERMOTOPHYTE TEST MEDIUM

K810181 · JSJ

Microbiology · 14d

Troy Biologicals, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Troy Biologicals, Inc.

Filters