Last synced on 25 April 2025 at 11:05 pm

CLEAR-GUARD MIDI, CLEAR-GUARD MIDI W/FLEXTUBE, CLEAR-THERM MINI, CLEAR-THERM MINI W/FLEXTUBE, MODELS 1644,1644-T,1831,18

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K983610
510(k) Type
Traditional
Applicant
INTERSURGICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/30/1999
Days to Decision
198 days
Submission Type
Statement

CLEAR-GUARD MIDI, CLEAR-GUARD MIDI W/FLEXTUBE, CLEAR-THERM MINI, CLEAR-THERM MINI W/FLEXTUBE, MODELS 1644,1644-T,1831,18

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K983610
510(k) Type
Traditional
Applicant
INTERSURGICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/30/1999
Days to Decision
198 days
Submission Type
Statement