Atlas FDA

BARTON-MAYO TRACHEOSTOMA BUTTON

FDA 510(k) clearance K901377 · decided 1990-06-14

Clearance details

K-number
K901377
Device name
BARTON-MAYO TRACHEOSTOMA BUTTON
Applicant
Medical Innovations International, Inc.
Decision
Substantially Equivalent
Date received
1990-03-22
Decision date
1990-06-14
Days to decision
84 days
Clearance type
Traditional
Product code
KAC
Device class
1
Regulation number
874.4420
Medical specialty
Ear, Nose, Throat
Advisory committee
Ear, Nose, Throat
Location
Rochester, MN, 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
LARYNGECTOMY TUBE (K873992)Portex, Inc.1988-03-24
SHILEY LARYNGECTOMY TUBE (K821993)Shiley, Inc.1982-08-12
NORTHWESTERN VOICE RESTORATION KIT (K811428)Universal Prosthetics, Inc.1981-06-16

Recalls involving this device

No recalls on record reference this clearance.