Rudolf Riester GmbH & Co. KG
Jungingen, DE
Rudolf Riester GmbH & Co. KG appears in FDA device records in Jungingen, DE. FDA records list 30 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.
FDA records held for this company
- 510(k) clearances
- 30
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 30 510(k) clearances for Rudolf Riester GmbH & Co. KG between 1993 and 2000. The busiest year on record is 1993, with 12. The most recent is 2000, with 2.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1993 | 12 |
| 1994 | 5 |
| 1995 | 6 |
| 1997 | 5 |
| 2000 | 2 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K002955 | EMPIRE N BLOOD PRESSURE MANOMETERS | DXQ | Substantially Equivalent | |
| K002954 | RI-SAN/RI-SANA BLOOD PRESSURE MANOMETERS | DXQ | Substantially Equivalent | |
| K972379 | PRECISA N | DXQ | Substantially Equivalent | |
| K972378 | SANAPHON N | DXQ | Substantially Equivalent | |
| K972377 | RI-MEGA | DXQ | Substantially Equivalent | |
| K972301 | BIG BEN SQUARE, BIG BEN ROUND | DXQ | Substantially Equivalent | |
| K964338 | RI-TINISCOPE-SLIT/RI-TINISCOPE SPOT/RI-VISION-SLIT/RI-VISION-SPOT | HKM | Substantially Equivalent | |
| K950914 | RI-FORMER WALL MODEL 2,5 V/220 V OR 110 V 3,5 V/220 V OR 110 V, RI-FORMER ANAESTHETIC MODEL 2,5 V/220 V OR 110 C 3,5 V/V | HLJ | Substantially Equivalent | |
| K950913 | PERFECT, ENT SET, PRAKTIKANT, DE LUXE | ERA | Substantially Equivalent | |
| K945541 | SCHIOTZ TONOMETER SPEC. 5 STRAIGHT, INCLINED, 3INCLINED SCALE | HKY | Substantially Equivalent | |
| K945425 | MCINTOSH, MILLER, FOREGGER BABY | CCW | Substantially Equivalent | |
| K946043 | H5000, H5000L, H5000L REVERSE MODEL H5000C, H5000CG | ERA | Unknown | |
| K945640 | RI-SCOPE S OTOSCOPE | HLJ | Unknown | |
| K945507 | H 5100, H 5200, H 5300 | KZF | Substantially Equivalent | |
| K942777 | MINIMUS II; MINIMUS II COLOR; BABYPHON | DXQ | Substantially Equivalent | |
| K925295 | EXACTA-SPEZIAL | DXN | Substantially Equivalent | |
| K925294 | PRECISA | DXN | Substantially Equivalent | |
| K925297 | RI-MED | DXQ | Substantially Equivalent | |
| K925755 | DE LUXE | HLJ | Unknown | |
| K925756 | UNI II | HLJ | Substantially Equivalent | |
| K932504 | RI-FORMER | HLJ | Unknown | |
| K932506 | RI-SCOPE (S) | ERA | Substantially Equivalent | |
| K932505 | RI-STAR | ERA | Substantially Equivalent | |
| K932503 | RI-MINI | ERA | Substantially Equivalent | |
| K925754 | ECONOM | EPY | Substantially Equivalent | |
| K925753 | UNI III | ERA | Substantially Equivalent | |
| K925752 | STANDARD | ERA | Substantially Equivalent | |
| K925758 | OTOSCOPE | ERA | Substantially Equivalent | |
| K925757 | OPHTHALMOSCOPE | HLJ | Substantially Equivalent | |
| K925759 | UNI I | ERA | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
Recall records
No recall records for this company in the ingested FDA data.
Verification record
There is no verification record for this company. Most companies on this site have none: a record exists only where a company asked to be verified and MDM ran the checks, so the absence of one says nothing about the company.
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Data as of , FDA export datePage updated Source: openFDA, public domain