Medical Device Manufacturer · US , Mchenry , IL

Propper Mfg. Co., Inc. - FDA 510(k) Cleared Devices

25 submissions · 25 cleared · Since 1977

25

Total

25

Cleared

0

Denied

FDA 510(k) Regulatory Record - Propper Mfg. Co., Inc. Hematology ✕

3 devices

1-3 of 3

Cleared Oct 05, 1992

PROPPER SUPER SERACULT(R)

Hematology · 174d

Cleared Jan 27, 1984

PROPPER SERACULT

Hematology · 50d

Cleared Jan 28, 1982

SERACULT OCCULT BLOOF TEST

Hematology · 76d