The following data is part of a premarket notification filed by Procedure Products, Inc. with the FDA for 10cc Syringe Control Ring Set.
| Device ID | K874747 |
| 510k Number | K874747 |
| Device Name: | 10CC SYRINGE CONTROL RING SET |
| Classification | Syringe, Piston |
| Applicant | PROCEDURE PRODUCTS, INC. 1801 WEST 4TH PLAIN BLVD. Vancouver, WA 98660 |
| Contact | Kurt George |
| Correspondent | Kurt George PROCEDURE PRODUCTS, INC. 1801 WEST 4TH PLAIN BLVD. Vancouver, WA 98660 |
| Product Code | FMF |
| CFR Regulation Number | 880.5860 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1987-11-18 |
| Decision Date | 1988-02-04 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| B160984930GR1 | K874747 | 000 |
| B1604930R1 | K874747 | 000 |
| B1604930G542 | K874747 | 000 |
| B1604930G1 | K874747 | 000 |
| B1604930B431 | K874747 | 000 |
| B1604930B1 | K874747 | 000 |
| B1604920G2 | K874747 | 000 |
| B1604410W2 | K874747 | 000 |
| B1604410G1 | K874747 | 000 |
| B1604930R431 | K874747 | 000 |
| B1604930R541 | K874747 | 000 |
| B1604930W871 | K874747 | 000 |
| B16098361 | K874747 | 000 |
| B1604950Y1 | K874747 | 000 |
| B1604950W872 | K874747 | 000 |
| B1604950G1 | K874747 | 000 |
| B1604930Y432 | K874747 | 000 |
| B1604930Y321 | K874747 | 000 |
| B1604930Y211 | K874747 | 000 |
| B1604930Y1 | K874747 | 000 |
| B1604410B1 | K874747 | 000 |