Ritmed, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ritmed, Inc. - FDA 510(k) Cleared Devices
22
Total
22
Cleared
0
Denied
Ritmed, Inc. has 22 FDA 510(k) cleared general & plastic surgery devices. Based in Mchenry, US.
Historical record: 22 cleared submissions from 1983 to 1984.
Browse the complete list of FDA 510(k) cleared general & plastic surgery devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Ritmed, Inc.
22 devices
Cleared
Feb 17, 1984
FLORET FOAM PREP SPONGE
General & Plastic Surgery
126d
Cleared
Sep 26, 1983
ISOVIS WOUND PROTECTOR
General Hospital
34d
Cleared
Jun 24, 1983
ISOVIS WOUND PROTECTOR
General Hospital
150d
Cleared
Jun 08, 1983
FLORET STRUNG GAUZE SPONGES
General & Plastic Surgery
134d
Cleared
Jun 08, 1983
FLORET KITTNER OR K DISSECTOR
General & Plastic Surgery
134d
Cleared
Jun 08, 1983
FLORET SPECIAL GAUZE SPONGES
General & Plastic Surgery
134d
Cleared
Jun 08, 1983
FLORET CYLINDRICAL/BRONCHOSCOPIC/LAMIN
General & Plastic Surgery
134d
Cleared
Jun 03, 1983
FLORET TONSIL & ADENOID SPONGES
General & Plastic Surgery
129d
Cleared
Jun 03, 1983
PROTET HOLDERS-BLOCKS & ROLL
General & Plastic Surgery
129d
Cleared
Jun 02, 1983
FLORET NEURO SPONGE
General & Plastic Surgery
128d
Cleared
Jun 02, 1983
LAPET & LAPWALL LAPAROTOMY SPONGES
General & Plastic Surgery
128d
Cleared
May 09, 1983
PROTET SOAP & WASH MITT
General & Plastic Surgery
104d