Medical Device Manufacturer · US , Mchenry , IL

R. A. Fischer Co. Corp. - FDA 510(k) Cleared Devices

13 submissions · 12 cleared · Since 1976

Total

Cleared

Denied

R. A. Fischer Co. Corp. has 12 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 12 cleared submissions from 1976 to 1997. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by R. A. Fischer Co. Corp. Filter by specialty or product code using the sidebar.

R. A. Fischer Co. Corp. 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 - R. A. Fischer Co. Corp.

13 devices

1-12 of 13

Cleared Apr 30, 1997

MD-1A GALVANIC UNIT

K964208 · EGJ

Physical Medicine · 208d

Cleared Jan 05, 1996

COMPU-BLEND EPILATOR

K954031 · KCW

General & Plastic Surgery · 130d

Cleared Jun 26, 1990

MD-2 IONTOPHORESIS UNIT

K895365 · EGJ

Physical Medicine · 302d

Cleared Jun 05, 1989

MODEL SE-5 EPILATOR

K893389 · KCW

General & Plastic Surgery · 35d

Cleared Oct 04, 1988

MODEL CBX EPILATOR

K884079 · KCW

General & Plastic Surgery · 7d

Cleared Apr 28, 1987

CB-7 ELECTRONIC EPILATOR

K871372 · KCW

General & Plastic Surgery · 21d

Cleared Nov 08, 1985

ULTRAVIOLET TREATMENT LAMPS UV-8 & UV-9

K852534 · FTC

General & Plastic Surgery · 147d

Cleared Sep 26, 1984

ELECTRONIC EPILATOR TS-1

K843063 · KCW

General & Plastic Surgery · 51d

Cleared Jan 14, 1983

HIGH FREQUENCY EPILATOR CB-2

K823674 · KCW

General & Plastic Surgery · 38d

Cleared Jul 28, 1980

EPILATOR, MODEL CP-16

K801351 · KCW

General & Plastic Surgery · 49d

Cleared Jan 24, 1978

EPILATOR, ELECTRONIC MODEL SE-2

K780076 · KCW

General & Plastic Surgery · 8d

Cleared Feb 17, 1977

STIMULATOR, ELECTRICAL MUSCLE (#MD-4)

K760547 · IPF

Physical Medicine · 171d

R. A. Fischer Co. Corp. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - R. A. Fischer Co. Corp.

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