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MODEL GT1ST CRYOSURGICAL INSTRUMENT

Page Type
Cleared 510(K)
510(k) Number
K922878
510(k) Type
Traditional
Applicant
GYNE-TECH INSTRUMENT CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/2/1992
Days to Decision
79 days
Submission Type
Statement

MODEL GT1ST CRYOSURGICAL INSTRUMENT

Page Type
Cleared 510(K)
510(k) Number
K922878
510(k) Type
Traditional
Applicant
GYNE-TECH INSTRUMENT CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/2/1992
Days to Decision
79 days
Submission Type
Statement