Atlas FDA

FALL-SAFE VEST

FDA 510(k) clearance K841672 · decided 1984-07-03

Clearance details

K-number
K841672
Device name
FALL-SAFE VEST
Applicant
Fsm Corp.
Decision
Substantially Equivalent
Date received
1984-04-23
Decision date
1984-07-03
Days to decision
71 days
Clearance type
Traditional
Product code
KMI
Device class
1
Regulation number
880.2400
Medical specialty
General Hospital
Advisory committee
General Hospital
Location
Mchenry, IL, US
Third-party review
No
Expedited review
No

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PM-PAGER (K933552)Hill Engineering1994-09-22
HOME AMB-ALERT (K934344)Medway1994-04-29
TELETOM (K940405)Berchtold Holding GmbH1994-04-14
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Recalls involving this device

No recalls on record reference this clearance.