STERI-TAMP
Container, I.v.
PHARMACY, INC.
The following data is part of a premarket notification filed by Pharmacy, Inc. with the FDA for Steri-tamp.
Pre-market Notification Details
| Device ID | K974180 |
| 510k Number | K974180 |
| Device Name: | STERI-TAMP |
| Classification | Container, I.v. |
| Applicant | PHARMACY, INC. 3234 ELLA LN. New Port Richey, FL 34655 |
| Contact | Ed Ransom |
| Correspondent | Ed Ransom PHARMACY, INC. 3234 ELLA LN. New Port Richey, FL 34655 |
| Product Code | KPE |
| CFR Regulation Number | 880.5025 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1997-11-06 |
| Decision Date | 1998-02-24 |
| Summary: | summary |
NIH GUDID Devices
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00858246002070 | K974180 | 000 |
| 00858246002063 | K974180 | 000 |
| 00858246002056 | K974180 | 000 |
| 00858246002049 | K974180 | 000 |
| 00858246002032 | K974180 | 000 |
| 00858246002025 | K974180 | 000 |
| 00858246002018 | K974180 | 000 |
| 00858246002001 | K974180 | 000 |
Trademark Results [STERI-TAMP]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 STERI-TAMP 85681488 4301116 Live/Registered |
ALLIED PHARMACY PRODUCTS, INC. 2012-07-19 |
 STERI-TAMP 75307234 2355636 Dead/Cancelled |
AMERICAN PHARMACEUTICAL PARTNERS, INC. 1997-06-11 |
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