The following data is part of a premarket notification filed by Espe Gmbh & Co. Kg. with the FDA for Permadyne Penta (high & Low Viscosity).
Device ID | K953027 |
510k Number | K953027 |
Device Name: | PERMADYNE PENTA (HIGH & LOW VISCOSITY) |
Classification | Material, Impression |
Applicant | ESPE GMBH & CO. KG. AM GRIESBERG 2 Seefeld, DE D-82229 |
Contact | Barbara Wagner |
Correspondent | Barbara Wagner ESPE GMBH & CO. KG. AM GRIESBERG 2 Seefeld, DE D-82229 |
Product Code | ELW |
CFR Regulation Number | 872.3660 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1995-06-29 |
Decision Date | 1995-07-19 |