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KARL STORZ SUBGLOTTISCOPE, NEONATE AND INFANT, FIBER OPTIC LIGHT CARRIER, SUCTION TUBE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K951804
510(k) Type
Traditional
Applicant
KARL STORZ ENDOSCOPY-AMERICA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/5/1995
Days to Decision
47 days
Submission Type
Summary

KARL STORZ SUBGLOTTISCOPE, NEONATE AND INFANT, FIBER OPTIC LIGHT CARRIER, SUCTION TUBE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K951804
510(k) Type
Traditional
Applicant
KARL STORZ ENDOSCOPY-AMERICA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/5/1995
Days to Decision
47 days
Submission Type
Summary