The following data is part of a premarket notification filed by Haemonetics Corp. with the FDA for Orthopedic Wound Drainage Set With Trocar.
Device ID | K893394 |
510k Number | K893394 |
Device Name: | ORTHOPEDIC WOUND DRAINAGE SET WITH TROCAR |
Classification | Apparatus, Autotransfusion |
Applicant | HAEMONETICS CORP. 400 WOOD RD. P.O. BOX 9114 Braintree, MA 02184 |
Contact | Michael Mathews |
Correspondent | Michael Mathews HAEMONETICS CORP. 400 WOOD RD. P.O. BOX 9114 Braintree, MA 02184 |
Product Code | CAC |
CFR Regulation Number | 868.5830 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1989-05-01 |
Decision Date | 1989-10-19 |