Atlas FDA

LEAP FROG

FDA 510(k) clearance K834211 · decided 1984-06-05

Clearance details

K-number
K834211
Device name
LEAP FROG
Applicant
Philips Medical Systems (Cleveland), Inc.
Decision
Substantially Equivalent
Date received
1983-12-05
Decision date
1984-06-05
Days to decision
183 days
Clearance type
Traditional
Product code
DSI
Device class
2
Regulation number
870.1025
Medical specialty
Cardiovascular
Advisory committee
Cardiovascular
Location
Walker, MI, US
Third-party review
No
Expedited review
No

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Recalls involving this device

No recalls on record reference this clearance.

PMA approvals by this applicant

RecordFirmDate
NUCLEAR MAGNETIC RESONANCE SCANNER MODELS NMR 1000 (P830052/S019)Philips Medical Systems (Cleveland), Inc.1988-07-27
NUCLEAR MAGNETIC RESONANCE SCANNER MODELS NMR 1000 (P830052/S022)Philips Medical Systems (Cleveland), Inc.1988-07-14
NUCLEAR MAGNETIC RESONANCE SCANNER MODELS NMR 1000 (P830052/S021)Philips Medical Systems (Cleveland), Inc.1988-07-14
NUCLEAR MAGNETIC RESONANCE SCANNER MODELS NMR 1000 (P830052/S018)Philips Medical Systems (Cleveland), Inc.1988-06-13
NUCLEAR MAGNETIC RESONANCE SCANNER MODELS NMR 1000 (P830052/S017)Philips Medical Systems (Cleveland), Inc.1988-05-16
NUCLEAR MAGNETIC RESONANCE SCANNER MODELS NMR 1000 (P830052/S015)Philips Medical Systems (Cleveland), Inc.1988-05-16
NUCLEAR MAGNETIC RESONANCE SCANNER MODELS NMR 1000 (P830052/S016)Philips Medical Systems (Cleveland), Inc.1988-04-28
NUCLEAR MAGNETIC RESONANCE SCANNER MODELS NMR 1000 (P830052/S014)Philips Medical Systems (Cleveland), Inc.1988-04-26