DERMAPIK
System, Delivery, Allergen And Vaccine
CREATIVE SCIENTIFIC EQUIPMENT CORP.
The following data is part of a premarket notification filed by Creative Scientific Equipment Corp. with the FDA for Dermapik.
Pre-market Notification Details
| 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 |
Trademark Results [DERMAPIK]
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 |
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