The following data is part of a premarket notification filed by Marlo Surgical Technology with the FDA for Flynn Tissue Probe And Blunt Dissector.
Device ID | K910713 |
510k Number | K910713 |
Device Name: | FLYNN TISSUE PROBE AND BLUNT DISSECTOR |
Classification | Laparoscope, Gynecologic (and Accessories) |
Applicant | MARLO SURGICAL TECHNOLOGY 1810 JOSEPH LLOYD PKWY. Willoughby, OH 44094 |
Contact | Scott C Marlow |
Correspondent | Scott C Marlow MARLO SURGICAL TECHNOLOGY 1810 JOSEPH LLOYD PKWY. Willoughby, OH 44094 |
Product Code | HET |
CFR Regulation Number | 884.1720 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1991-02-20 |
Decision Date | 1991-03-21 |