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REGALTECH MAXISCOPE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K921163
510(k) Type
Traditional
Applicant
REGALTECH PTY. LTD.
Country
Australia
FDA Decision
Substantially Equivalent
Decision Date
10/27/1992
Days to Decision
230 days
Submission Type
Statement

REGALTECH MAXISCOPE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K921163
510(k) Type
Traditional
Applicant
REGALTECH PTY. LTD.
Country
Australia
FDA Decision
Substantially Equivalent
Decision Date
10/27/1992
Days to Decision
230 days
Submission Type
Statement