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X-Cel X-Ray Corp

Crystal Lake, IL, US

X-CEL X-RAY CORP. appears in FDA device records in Crystal Lake, IL. FDA records list 4 510(k) clearances between and , no PMA records and one registered establishment. As of , FDA records show one recall for this company, and at least one establishment registration is current.

FDA records held for this company

510(k) clearances
4
PMA records
0
Recall records
1
Registered establishments
1

510(k) clearance history

FDA records hold 4 510(k) clearances for X-Cel X-Ray Corp between 1981 and 2000. The busiest year on record is 1981, with 1. The most recent is 2000, with 1.

Clearances by year, as a table
510(k) clearance decisions for X-Cel X-Ray Corp, by decision year
YearClearances
19811
19871
19931
20001
510(k) clearances on record, most recent first
K numberDeviceProduct codeDecisionDecision date
K993958IDX-60 INTRAORAL X-RAYMUHSubstantially Equivalent
K930699M6-MIZLSubstantially Equivalent
K871116X-CEL X-RAY MODELS ORT90W, ORT90M AND ORT90RIYHSubstantially Equivalent
K811230X-CELL X-RAY #'S P-75W/P-75MKPRSubstantially Equivalent

Registered establishments

FDA registered establishments for X-Cel X-Ray Corp, with the product codes listed at each
RegistrationFEIEstablishmentAddressRegistration expiresProduct codes listed
14184841418484X-CEL X-RAY CORP.4220 WALLER ST, Crystal Lake, IL 60012 US2026

Registration numbers link to the FDA registration and listing record for that establishment.

FDA product codes

Recall records

Device recall records naming this company, most recent first
RecallProductReasonClassificationInitiatedStatus
Z-0424-03X-Cel MB-700 A/C Podiatry X-Ray System; X-Cel X-Ray Coporation, 4220 Waller Drive, Crystal Lake, IL 60012The X-Ray system contained a defective X-Ray tube shield.Terminated

Verification record

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Data as of , FDA export datePage updated Source: openFDA, public domain