Atlas FDA

ND. YAG LASER FOR ENDOBRONCHIAL OBSTRUC

FDA 510(k) clearance K843228 · decided 1984-09-04

Clearance details

K-number
K843228
Device name
ND. YAG LASER FOR ENDOBRONCHIAL OBSTRUC
Applicant
Endo Lase, Inc.
Decision
Substantially Equivalent
Date received
1984-08-16
Decision date
1984-09-04
Days to decision
19 days
Clearance type
Traditional
Advisory committee
Unknown
Location
Mchenry, IL, US
Third-party review
No
Expedited review
No

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Recalls involving this device

No recalls on record reference this clearance.