Medical Device Manufacturer · US , Grayson , GA

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

10 submissions · 10 cleared · Since 1997

Total

Cleared

Denied

Lee Laboratories, Inc. has 10 FDA 510(k) cleared microbiology devices. Based in Grayson, US.

Historical record: 10 cleared submissions from 1997 to 1997.

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

Lee 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 - Lee Laboratories, Inc.

10 devices

1-10 of 10

Cleared Aug 25, 1997

VISTA ANTIGEN SALMONELLA O GROUP B

K972386 · GNC

Microbiology · 60d

Cleared Aug 25, 1997

VISTA ANTIGEN SALMONELLA O GROUP A

K972387 · GNC

Microbiology · 60d

Cleared Aug 25, 1997

VISTA ANTIGEN SALMONELLA O GROUP C

K972388 · GNC

Microbiology · 60d

Cleared Aug 25, 1997

VISTA ANTIGEN SALMONELLA H D

K972389 · GNC

Microbiology · 60d

Cleared Aug 25, 1997

VISTA ANTIGEN SALMONELLA H C

K972390 · GNC

Microbiology · 60d

Cleared Aug 25, 1997

VISTA ANTIGEN SALMONELLA H B

K972391 · GNC

Microbiology · 60d

Cleared Aug 25, 1997

VISTA ANTIGEN SALMONELLA H A

K972392 · GNC

Microbiology · 60d

Cleared Aug 25, 1997

VISTA ANTIGEN BRUCELLA ABORTUS

K972394 · GSO

Microbiology · 60d

Cleared Aug 25, 1997

VISTA ANTIGEN SALMONELLA O GROUP D

K972395 · GNC

Microbiology · 60d

Cleared Aug 25, 1997

VISTA ANTIGEN BRUCELLA MELITENSIS

K972396 · GSO

Microbiology · 60d

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

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

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