Panpac Medical Corporation
Shi-Chih City, Taipei Hsien, TW
Panpac Medical Corporation appears in FDA device records in Shi-Chih City, Taipei Hsien, TW. FDA records list 12 510(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
- 12
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 12 510(k) clearances for Panpac Medical Corporation between 2010 and 2018. The busiest year on record is 2010, with 5. The most recent is 2018, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 2010 | 5 |
| 2011 | 1 |
| 2013 | 1 |
| 2014 | 2 |
| 2016 | 1 |
| 2017 | 1 |
| 2018 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K173351 | Panpac Flexi Shelf Pessary | HHW | Substantially Equivalent | |
| K161106 | PANPAC DISPOSABLE VACUUM CURETTES | HGH | Substantially Equivalent | |
| K153422 | Panpac Disposable Pessary Fitting Set | HHW | Substantially Equivalent | |
| K132670 | PANPAC INFLATABLE DOCUT PESSARY | HHW | Substantially Equivalent | |
| K130087 | PANPAC WORD/BARTHOLIN CATHETER | KNA | Substantially Equivalent | |
| K130273 | PANPAC VAGINAL DILATORS | HDX | Substantially Equivalent | |
| K102898 | BELLOTA SONOHYSTEROGRAPHY CATHETER WITH CERVICAL CONE, BELLOTA SONOHYSTEROGRAPHY CATHETER WITHOUT CERVICAL CONE | LKF | Substantially Equivalent | |
| K092982 | THE PANPAC SUCTION CURETTE | HHK | Substantially Equivalent | |
| K092981 | PANPAC VAGINAL PESSARY | HHW | Substantially Equivalent | |
| K092983 | PANPAC HSG CATHETER SET | LKF | Substantially Equivalent | |
| K092984 | PANPAC UTERINE INECTOR, MODEL UI-4.0, UI-2.0 | LKF | Substantially Equivalent | |
| K092980 | PANPAC UTERINE MANIPULATOR INJECTOR, MODEL UMI 4.5 | LKF | 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