The following data is part of a premarket notification filed by Rnk Products, Inc. with the FDA for Pcp/pc Stethoscope.
| Device ID | K102893 |
| 510k Number | K102893 |
| Device Name: | PCP/PC STETHOSCOPE |
| Classification | Stethoscope, Electronic |
| Applicant | RNK PRODUCTS, INC. 4195 US HWY 1 SUITE 101 Rockledge, FL 32955 |
| Contact | Charles R Abbruscato |
| Correspondent | Charles R Abbruscato RNK PRODUCTS, INC. 4195 US HWY 1 SUITE 101 Rockledge, FL 32955 |
| Product Code | DQD |
| CFR Regulation Number | 870.1875 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2010-09-30 |
| Decision Date | 2011-01-20 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00067799300216 | K102893 | 000 |
| 00677986002016 | K102893 | 000 |