Atlas FDA

WECK-LUBE, CATALOG NO. 850-150

FDA 510(k) clearance K861591 · decided 1986-05-23

Clearance details

K-number
K861591
Device name
WECK-LUBE, CATALOG NO. 850-150
Applicant
Palmetto Chemical & Supply Co., Inc.
Decision
Substantially Equivalent
Date received
1986-04-29
Decision date
1986-05-23
Days to decision
24 days
Clearance type
Traditional
Advisory committee
Unknown
Location
Monroe, NC, US
Third-party review
No
Expedited review
No

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Recalls involving this device

No recalls on record reference this clearance.