Medical Device Manufacturer · US , Mchenry , IL

F. & F. Koenigkramer - FDA 510(k) Cleared Devices

9 submissions · 9 cleared · Since 1977

Total

Cleared

Denied

F. & F. Koenigkramer has 9 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 9 cleared submissions from 1977 to 1986. Primary specialty: Ophthalmic.

Browse the FDA 510(k) cleared devices submitted by F. & F. Koenigkramer Filter by specialty or product code using the sidebar.

F. & F. Koenigkramer 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 - F. & F. Koenigkramer

9 devices

1-9 of 9

Cleared Feb 19, 1986

RELIANCE MODEL 200 PODIATRY CHAIR

K860519 · LGX

General Hospital · 8d

Cleared Sep 05, 1985

RELIANCE 1000, RELIANCE 1500, RELIANCE 2000

RELIANCE TREATMENT CABINET

K843046 · ETF

Ear, Nose, Throat · 56d

Cleared Feb 04, 1984

RELIANCE OPHTHALMIC SLIT LAMP R-083

K834060 · HQF

Ophthalmic · 71d

Cleared Jun 30, 1983

RELIANCE TEMPO OPHTH. INSTR STAND

K831568 · HHF

Obstetrics & Gynecology · 45d

Cleared Sep 21, 1981

RELIANCE OPHTHALMIC INSTRUMENT CONTROL

K812544 · HMF

Ophthalmic · 17d

Cleared Jan 28, 1977

RELIANCE MOD-U-LINE M-700

K761147 · FPO

General Hospital · 63d

F. & F. Koenigkramer - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - F. & F. Koenigkramer

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