Atlas FDA

TEMP. PROBE, & ELECTRONIC THERMOMETER

FDA 510(k) clearance K770341 · decided 1977-02-28

Clearance details

K-number
K770341
Device name
TEMP. PROBE, & ELECTRONIC THERMOMETER
Applicant
Electro-Catheter Corp.
Decision
Substantially Equivalent
Date received
1977-02-18
Decision date
1977-02-28
Days to decision
10 days
Clearance type
Traditional
Product code
DRF
Device class
2
Regulation number
870.1220
Medical specialty
Cardiovascular
Advisory committee
Cardiovascular
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.