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THE TULIP LCI-200 ILLUMINATION & IMAGING SYSTEM (MODIFICATION)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K954734
510(k) Type
Traditional
Applicant
THE TULIP MFG. CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/14/1995
Days to Decision
42 days
Submission Type
Summary

THE TULIP LCI-200 ILLUMINATION & IMAGING SYSTEM (MODIFICATION)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K954734
510(k) Type
Traditional
Applicant
THE TULIP MFG. CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/14/1995
Days to Decision
42 days
Submission Type
Summary