The following data is part of a premarket notification filed by Intl. Medical Industries with the FDA for Tamper Proof Cap.
| Device ID | K861276 |
| 510k Number | K861276 |
| Device Name: | TAMPER PROOF CAP |
| Classification | Syringe, Piston |
| Applicant | INTL. MEDICAL INDUSTRIES 570 PLEASANT ST. Watertown, MA 02172 |
| Contact | John P Vitello |
| Correspondent | John P Vitello INTL. MEDICAL INDUSTRIES 570 PLEASANT ST. Watertown, MA 02172 |
| Product Code | FMF |
| CFR Regulation Number | 880.5860 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1986-04-07 |
| Decision Date | 1986-05-05 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| B212TEC10W2 | K861276 | 000 |
| B21217360W2 | K861276 | 000 |
| B21217360RC2 | K861276 | 000 |
| B21217360R2 | K861276 | 000 |
| B21217360KC2 | K861276 | 000 |
| B21217360K2 | K861276 | 000 |
| B21217360BC2 | K861276 | 000 |
| B21217360B2 | K861276 | 000 |
| B21257351W2 | K861276 | 000 |
| B21257351R2 | K861276 | 000 |
| B21257351B2 | K861276 | 000 |
| B21257301W2 | K861276 | 000 |
| B21257301R2 | K861276 | 000 |
| B21257301B2 | K861276 | 000 |
| B21257261002 | K861276 | 000 |
| B21257251002 | K861276 | 000 |
| B21257241002 | K861276 | 000 |
| B21257302SCA2 | K861276 | 000 |
| B21217360WC2 | K861276 | 000 |
| B21217361R2 | K861276 | 000 |
| B2125724CE1 | K861276 | 000 |
| B212TEC10B2 | K861276 | 000 |
| B212TEC102 | K861276 | 000 |
| B212ISOTECW2 | K861276 | 000 |
| B212ISOTECR2 | K861276 | 000 |
| B212ISOTECB2 | K861276 | 000 |
| B2125780W2 | K861276 | 000 |
| B2125780K2 | K861276 | 000 |
| B2125780B2 | K861276 | 000 |
| B21257802 | K861276 | 000 |
| B21257642 | K861276 | 000 |
| B2125750W2 | K861276 | 000 |
| B2125750R1 | K861276 | 000 |
| B2125750K2 | K861276 | 000 |
| B2125750B2 | K861276 | 000 |
| B21257302 | K861276 | 000 |
| B2125726CE2 | K861276 | 000 |
| B2125725CE2 | K861276 | 000 |
| B2125726SCA2 | K861276 | 000 |