Atlas FDA

MYELOGRAM PROCEDURE TRAY

FDA 510(k) clearance K852501 · decided 1985-07-11

Clearance details

K-number
K852501
Device name
MYELOGRAM PROCEDURE TRAY
Applicant
Manan Manufacturing Co., Inc.
Decision
Unknown
Date received
1985-06-12
Decision date
1985-07-11
Days to decision
29 days
Clearance type
Traditional
Advisory committee
Unknown
Location
Skokie, IL, US
Third-party review
No
Expedited review
No

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Recalls involving this device

No recalls on record reference this clearance.