The following data is part of a premarket notification filed by Creative Scientific Equipment Corp. with the FDA for Dermapik.
Device ID | K882360 |
510k Number | K882360 |
Device Name: | DERMAPIK |
Classification | System, Delivery, Allergen And Vaccine |
Applicant | CREATIVE SCIENTIFIC EQUIPMENT CORP. 3711 LONG BEACH BLVD. Long Beach, CA 90807 |
Contact | Pitesky, Md |
Correspondent | Pitesky, Md CREATIVE SCIENTIFIC EQUIPMENT CORP. 3711 LONG BEACH BLVD. Long Beach, CA 90807 |
Product Code | LDH |
CFR Regulation Number | 510(k) Premarket Notification [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1988-06-07 |
Decision Date | 1988-08-09 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
DERMAPIK 75352104 2512939 Dead/Cancelled |
Pitesky, Isadore 1997-09-05 |
DERMAPIK 73799161 1576007 Dead/Cancelled |
GREER LABORATORIES, INC. 1989-05-08 |
DERMAPIK 73381929 not registered Dead/Abandoned |
CREATIVE SCIENTIFIC EQUIPMENTCORPORATION 1982-08-26 |