Atlas FDA

CLINIX-R TOMOGRAPHIC DEVICE

FDA 510(k) clearance K810274 · decided 1981-03-11

Clearance details

K-number
K810274
Device name
CLINIX-R TOMOGRAPHIC DEVICE
Applicant
Philips Medical Systems (Cleveland), Inc.
Decision
Substantially Equivalent
Date received
1981-02-02
Decision date
1981-03-11
Days to decision
37 days
Clearance type
Traditional
Product code
IZF
Device class
2
Regulation number
892.1740
Medical specialty
Radiology
Advisory committee
Radiology
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.

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