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REGENT BIOGEL DIAGNOSTIC PROCEDURE GLOVE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K971514
510(k) Type
Traditional
Applicant
LONDON INTERNATIONAL GROUP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/29/1997
Days to Decision
187 days
Submission Type
Statement

REGENT BIOGEL DIAGNOSTIC PROCEDURE GLOVE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K971514
510(k) Type
Traditional
Applicant
LONDON INTERNATIONAL GROUP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/29/1997
Days to Decision
187 days
Submission Type
Statement