Atlas FDA

COMPTAR III

FDA 510(k) clearance K813051 · decided 1981-11-24

Clearance details

K-number
K813051
Device name
COMPTAR III
Applicant
Cgr Medical Corp.
Decision
Substantially Equivalent
Date received
1981-10-29
Decision date
1981-11-24
Days to decision
26 days
Clearance type
Traditional
Product code
IZO
Device class
1
Regulation number
892.1700
Medical specialty
Radiology
Advisory committee
Radiology
Location
Mchenry, IL, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
MPH50, MPH65, AND MPH80 (K954666)GE Medical Systems1995-11-24
HFX350, 30KW, 300MA, 1 OR 3 PHASE RADIOGRAPHIC & FLUOROSCOPIC X-RAY GENERATOR (K953582)Varian Canada, Inc.1995-09-26
N 800 HF (K953831)Nucletron-Oldelft Corp.1995-09-08
SHIMADZU X-RAY HIGH VILTAGE GENERATOR AHD150G (K952822)Shimadzu Corp.1995-07-12
MILESTONW 350/450/550HF, PCX N350/450/550HF, TOP-X 350/450/550HF RADIOGRAPHIC X-RAY GENERATOR (K952265)Control-X, Inc.1995-07-06
POLYDOROS SX 65 AND 80 (K950883)Siemens Medical Solutions USA, Inc.1995-04-03
COMPACT-X (K950694)Electromed Intl., Ltd.1995-03-31
DIGITAL 625HF (K950291)Fischer Imaging Corp.1995-03-23
UD 150L-R II (K945453)Shimadzu Medical Systems1995-03-21
SII 525 APR (K950040)Scott Imaging Intl., Inc.1995-03-21
SII 360 APR (K950041)Scott Imaging Intl., Inc.1995-03-21
UD 150L-F (K945452)Shimadzu Medical Systems1995-03-21

Recalls involving this device

No recalls on record reference this clearance.