Atlas FDA

INVOTEC SEPTAL BUTTON

FDA 510(k) clearance K901366 · decided 1990-06-14

Clearance details

K-number
K901366
Device name
INVOTEC SEPTAL BUTTON
Applicant
Invotec International, Inc.
Decision
Substantially Equivalent
Date received
1990-03-23
Decision date
1990-06-14
Days to decision
83 days
Clearance type
Traditional
Product code
LFB
Device class
U
Medical specialty
Unknown
Advisory committee
Unknown
Location
Jacksonville, FL, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
BLOM-SINGER SEPTAL PERFORATION PROSTHESIS (K131745)Helix Medical, LLC2013-09-17
SILMED NASAL SEPTAL BUTTON (K013696)Silmed, Inc.2001-11-28
MICROMEDICS NASAL SEPTAL BUTTON (K982667)Micromedics, Inc.1998-11-24
NASAL SEPTAL BUTTON (K972060)Boston Medical Products, Inc.1997-07-03
HOOD NASAL SEPTAL BUTTON (K920994)Hood Laboratories1992-05-15
OMEGA NASAL SEPTAL BUTTON (K871072)Omega Silicone, Inc.1987-06-08
CUI NASAL SEPTUM BUTTON (K871200)Cox-Uphuff Intl.1987-04-15
MICROTEK SEPTAL BUTTON (K862497)Microtek Medical, Inc.1986-07-14
NASAL SEPTAL BUTTON (K850492)Santa Barbara Medco, Inc.1985-03-07
NASAL SEPTAL BUTTONS (K822637)Abco Dealers, Inc.1982-09-28
SEPTAL BUTTON (K781529)Xomed, Inc.1978-10-17

Recalls involving this device

No recalls on record reference this clearance.