FDA.report

510(k) K992053

Device
AESCULAP VASCULAR INSTRUMENTS
Applicant
AESCULAP, INC.
510(k) number
K992053
Product code
DXC  
Decision
Substantially Equivalent (SESE)
Decision date
2000-01-13
Date received
1999-06-18
Regulation
870.4450
Classification name
Clamp, Vascular
Medical specialty
Cardiovascular
Review panel
Cardiovascular
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No
Source
FDA openFDA 510(k) dataset plus migrated FDA.report data

Related Records

Applicant Contact

Contact
MARY ELLEN HOLDEN
Address
1000 Gateway Blvd. South San Francisco CA US 94080 94080

FDA Registration Numbers

Source Documents

FDA 510(k) Premarket Notification Database · 510(k) summary PDF · openFDA JSON

Legacy Summary

summary

FDA Review

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