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COHERENT VERSAPULSE 2.1U /1.06U COMPACT SURGICAL LASER, MODELS A & B

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K933318
510(k) Type
Traditional
Applicant
LUMENIS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/8/1994
Days to Decision
354 days
Submission Type
Summary

COHERENT VERSAPULSE 2.1U /1.06U COMPACT SURGICAL LASER, MODELS A & B

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K933318
510(k) Type
Traditional
Applicant
LUMENIS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/8/1994
Days to Decision
354 days
Submission Type
Summary