Atlas FDA

TRANSCUTANEOUS ELECT. NERVE STIMULATOR

FDA 510(k) clearance K803247 · decided 1981-03-20

Clearance details

K-number
K803247
Device name
TRANSCUTANEOUS ELECT. NERVE STIMULATOR
Applicant
Medical Research Laboratories, Inc.
Decision
Substantially Equivalent
Date received
1980-12-23
Decision date
1981-03-20
Days to decision
87 days
Clearance type
Traditional
Advisory committee
Unknown
Location
Mchenry, IL, US
Third-party review
No
Expedited review
No

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Recalls involving this device

No recalls on record reference this clearance.