Last synced on 2 December 2022 at 11:04 pm

SUPER K-AMP, EZ-COMPRESSION, TRIM-PRO, HF-PRO, ENVIRO-PRO, COMPRESSION-PRO, COMPRESSION 3000, HF 3000, OCTIVA, REFLEX HF

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K964657
510(k) Type
Traditional
Applicant
MICRO-EAR TECHNOLOGY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/11/1997
Days to Decision
83 days
Submission Type
Statement