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PLM SENSOR, MODEL PLM1

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K940014
510(k) Type
Traditional
Applicant
PRO-TECH, INC.
Country
United States
FDA Decision
Substantially Equivalent - Subject to Tracking Regulation
Decision Date
11/10/1994
Days to Decision
310 days
Submission Type
Statement

PLM SENSOR, MODEL PLM1

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K940014
510(k) Type
Traditional
Applicant
PRO-TECH, INC.
Country
United States
FDA Decision
Substantially Equivalent - Subject to Tracking Regulation
Decision Date
11/10/1994
Days to Decision
310 days
Submission Type
Statement