The following data is part of a premarket notification filed by Pilling Co. with the FDA for Laser Bronchoscope System.
| Device ID | K861921 |
| 510k Number | K861921 |
| Device Name: | LASER BRONCHOSCOPE SYSTEM |
| Classification | Laser, Neodymium:yag, Pulmonary Surgery |
| Applicant | PILLING CO. 420 DELAWARE DR. Fort Washington, PA 19034 |
| Contact | Leland J Wimer |
| Correspondent | Leland J Wimer PILLING CO. 420 DELAWARE DR. Fort Washington, PA 19034 |
| Product Code | LLO |
| CFR Regulation Number | 874.4500 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1986-05-19 |
| Decision Date | 1986-06-02 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 24026704715569 | K861921 | 000 |
| 24026704715422 | K861921 | 000 |
| 24026704715415 | K861921 | 000 |
| 24026704715408 | K861921 | 000 |
| 24026704715392 | K861921 | 000 |
| 24026704715385 | K861921 | 000 |
| 24026704715378 | K861921 | 000 |
| 24026704715361 | K861921 | 000 |
| 24026704715354 | K861921 | 000 |
| 24026704715347 | K861921 | 000 |
| 34026704535690 | K861921 | 000 |
| 34026704535683 | K861921 | 000 |
| 24026704715439 | K861921 | 000 |
| 24026704715446 | K861921 | 000 |
| 24026704715552 | K861921 | 000 |
| 24026704715545 | K861921 | 000 |
| 24026704715538 | K861921 | 000 |
| 24026704715521 | K861921 | 000 |
| 14026704715517 | K861921 | 000 |
| 24026704715507 | K861921 | 000 |
| 24026704715491 | K861921 | 000 |
| 24026704715484 | K861921 | 000 |
| 24026704715477 | K861921 | 000 |
| 24026704715460 | K861921 | 000 |
| 24026704715453 | K861921 | 000 |
| 24026704536065 | K861921 | 000 |