Atlas FDA

SEERAM BLADE

FDA 510(k) clearance K844073 · decided 1984-11-19

Clearance details

K-number
K844073
Device name
SEERAM BLADE
Applicant
Seeram Products Development
Decision
Substantially Equivalent
Date received
1984-10-19
Decision date
1984-11-19
Days to decision
31 days
Clearance type
Traditional
Advisory committee
Unknown
Location
Vero Beach, FL, US
Third-party review
No
Expedited review
No

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Recalls involving this device

No recalls on record reference this clearance.