Atlas FDA

X-RAY APRON

FDA 510(k) clearance K870563 · decided 1987-02-19

Clearance details

K-number
K870563
Device name
X-RAY APRON
Applicant
X-Tech, Ltd.
Decision
Substantially Equivalent
Date received
1987-02-10
Decision date
1987-02-19
Days to decision
9 days
Clearance type
Traditional
Product code
EAJ
Device class
1
Regulation number
892.6500
Medical specialty
Radiology
Advisory committee
Radiology
Location
Newburyport, MA, 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
LEAD APRON (K931269)Bt Medical Co., Inc.1993-06-02
RINN PROTECTIVE X-RAY APRON AND PROTECTIVE COLLAR (K913621)Rinn Dental Products1991-09-27
LEAD APRON CADDY (K870103)Orthopedic Systems, Inc.1987-01-21
THYROID PROTECTIVE COLLAR (K832602)E.M. Adams1983-09-29
LEADED X-RAY APRON (K832601)E.M. Adams1983-09-29

Recalls involving this device

No recalls on record reference this clearance.