MYRINGOTOMY TUBE— 510(k) K971943
Substantially EquivalentMednet Locator, Inc.
FDA 510(k) clearance K971943 for MYRINGOTOMY TUBE, Substantially Equivalent on 1997-07-23. Applicant: Mednet Locator, Inc.. Device class: 2.
Clearance details
- Applicant
- Mednet Locator, Inc.
- Product code
- Code ETD
- Device class
- Class 2
- Regulation
- 21 CFR 874.3880
- Advisory panel
- Ear, Nose, Throat
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Memphis, TN, US
Recent devices under product code ETD
view all- K252436 — Tula Tympanostomy Tube Delivery Device
- K250256 — Solo+ Tympanostomy Tube Device (TTD), Solo+ TTD, Solo+ (Solo+ Tympanostomy Tube Handpiece (Catalogue #: 12115-100-000) and Solo+ Tympanostomy Tube Cartridge (Catalogue #: 12115-200-000))
- K232702 — Solo+ Tympanostomy Tube Device (TTD)
- K233658 — Biowy Tym Tube (TT)
- K232059 — Tympanostomy Tubes
More clearances from Mednet Locator, Inc.
view all- K001404 — GOLD TOTAL AND PARTIAL, REGULAR AND OFFSET, OSSICULAR REPLACEMENT PROSTHESES, GOLD TOTAL WITH FOUNTIAN HEAD, GOLD PISTON
- K001406 — HA/GOLD TOTAL AND PARTIAL, REGULAR AND OFFSET, OSSICULAR REPLACEMENT PROSTHESES
- K974174 — ULTRABUR
- K972734 — PARTIAL OSSICULAR REPLACEMENT PROSTHESIS (PORP)
- K972735 — TOTAL OSSICULAR REPLACEMENT PROSTHESIS (TORP)
Data sourced from openFDA. This site is unofficial and independent of the FDA.