Atlas FDA

C.S.M. HIP

FDA 510(k) clearance K862752 · decided 1986-08-07

Clearance details

K-number
K862752
Device name
C.S.M. HIP
Applicant
Protek, Inc.
Decision
Substantially Equivalent
Date received
1986-07-22
Decision date
1986-08-07
Days to decision
16 days
Clearance type
Traditional
Advisory committee
Unknown
Location
Indianapolis, IN, US
Third-party review
No
Expedited review
No

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Recalls involving this device

No recalls on record reference this clearance.