Atlas FDA

LIMB HOLDER, TECNOL REMINDER

FDA 510(k) clearance K760309 · decided 1976-08-09

Clearance details

K-number
K760309
Device name
LIMB HOLDER, TECNOL REMINDER
Applicant
Tecnol New Jersey Wound Care, Inc.
Decision
Substantially Equivalent
Date received
1976-07-26
Decision date
1976-08-09
Days to decision
14 days
Clearance type
Traditional
Advisory committee
Unknown
Location
Hammonton, NJ, US
Third-party review
No
Expedited review
No

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Recalls involving this device

No recalls on record reference this clearance.