The following data is part of a premarket notification filed by Adept-med Intl., Inc. with the FDA for Goott Multipurpose Flexible Retractor (sterile).
Device ID | K893869 |
510k Number | K893869 |
Device Name: | GOOTT MULTIPURPOSE FLEXIBLE RETRACTOR (STERILE) |
Classification | Retractor |
Applicant | ADEPT-MED INTL., INC. 3293 SARATOGA LN. PO BOX 1777 Cameron Park, CA 95682 |
Contact | Kathleen Quigley |
Correspondent | Kathleen Quigley ADEPT-MED INTL., INC. 3293 SARATOGA LN. PO BOX 1777 Cameron Park, CA 95682 |
Product Code | GAD |
CFR Regulation Number | 878.4800 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1989-05-26 |
Decision Date | 1989-08-03 |