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ULTRASONIC IMAGING SYSTEM (MODIFIED)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K860568
510(k) Type
Traditional
Applicant
INTERSPEC, INC.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
8/11/1986
Days to Decision
178 days

ULTRASONIC IMAGING SYSTEM (MODIFIED)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K860568
510(k) Type
Traditional
Applicant
INTERSPEC, INC.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
8/11/1986
Days to Decision
178 days