Medical Device Manufacturer · US , Allentown , NJ

Sita, Inc. - FDA 510(k) Cleared Devices

9 submissions · 9 cleared · Since 1987

Total

Cleared

Denied

Sita, Inc. has 9 FDA 510(k) cleared medical devices. Based in Allentown, US.

Historical record: 9 cleared submissions from 1987 to 1987. Primary specialty: Microbiology.

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

Sita, 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 - Sita, Inc.

9 devices

1-9 of 9

Cleared Oct 15, 1987

YHLAMYDIA CF ANTIGEN AND CONTROL ANTIGEN

K872700 · GPW

Microbiology · 100d

Cleared Sep 18, 1987

INFLUENZA B VIRUS CF ANTIGEN AND CONTROL ANTIGEN

K872693 · GNW

Microbiology · 73d

Cleared Sep 18, 1987

YNFLUENZA A VIRUS CF ANTIGEN AND CONTROL ANTIGEN

K872694 · GNW

Microbiology · 73d

Cleared Sep 18, 1987

PARAINFLUENZA-2-CF ANTIGEN AND CONTROL ANTIGEN

K872695 · GQT

Microbiology · 73d

Cleared Sep 18, 1987

PARAINFLUENZA-3-CF ANTIGEN AND CONTROL ANTIGEN

K872696 · GQT

Microbiology · 73d

Cleared Sep 18, 1987

PARAINFLUENZA-I-CF ANTIGEN AND CONTROL ANTIGEN

K872697 · GQT

Microbiology · 73d

Cleared Sep 18, 1987

ADENOVIRUS CF ANTIGEN AND CONTROL ANTIGEN

K872698 · GOA

Microbiology · 73d

Cleared Sep 18, 1987

MUMPS CF ANTIGEN AND CONTROL ANTIGEN

K872699 · GRB

Microbiology · 73d

Cleared Sep 18, 1987

RESPIRATORY SYNCYTIAL VIRUS CF ANTIGEN & CONTROL

K872701 · LKT

Microbiology · 73d

Sita, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Sita, Inc.

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