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PRO-LOK EXTENSION SET

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K933852
510(k) Type
Traditional
Applicant
BEECH MEDICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/29/1993
Days to Decision
145 days
Submission Type
Statement

PRO-LOK EXTENSION SET

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K933852
510(k) Type
Traditional
Applicant
BEECH MEDICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/29/1993
Days to Decision
145 days
Submission Type
Statement