Wisap Gesellschaft Fur Wissenschaftl. App. Bau mbH
Sauerlach, DE
Wisap Gesellschaft Fur Wissenschaftl. App. Bau Mbh appears in FDA device records in Sauerlach, DE. FDA records list 9 510(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
- 9
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 9 510(k) clearances for Wisap Gesellschaft Fur Wissenschaftl. App. Bau mbH between 1995 and 2003. The busiest year on record is 1999, with 3. The most recent is 2003, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1995 | 1 |
| 1997 | 1 |
| 1999 | 3 |
| 2000 | 2 |
| 2002 | 1 |
| 2003 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K031014 | HI-FLO THERME PNEU 45, WISAP #7083, 7083V | HIF | Substantially Equivalent | |
| K011510 | MULTI HI-FLO PNEU, WISAP #7080 | HIF | Substantially Equivalent | |
| K992513 | THERME-PNEU COMPUTER, WISAP #7070C, #7070CF, #7070CM, #7070CMF | HET | Substantially Equivalent | |
| K992481 | CO2-OP-PNEU COMPUTER, WISAP #7050C, #7050CF, #7050CMF | HET | Substantially Equivalent | |
| K990662 | DISPOSABLE HEATING TUBING SET #7642HSES | HIF | Substantially Equivalent | |
| K982515 | POWER-DRIVE, WISAP MODEL #7688PD/7688PD1 | HET | Substantially Equivalent | |
| K982518 | AQUA PURATOR-BIOTHERM, WISAP MODEL # 1608 | HET | Substantially Equivalent | |
| K960640 | S*E*M*M* SET FOR MOTO DRIVE WISAP #7689 SSM (MODIFICATION) | HET | Substantially Equivalent | |
| K952508 | FLOW-THERME, WISAP #7642 | HET | 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
