510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
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K972000Substantially Equivalent

X-Ray Assist Bar

Ralph Lindel, D.C., Great Neck, NY / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K972000 is the FDA 510(k) clearance record for X-RAY ASSIST BAR, a class II device, cleared for Ralph Lindel, D.C. on under FDA product code KPR (System, X-Ray, Stationary). FDA records list one 510(k) clearance for Ralph Lindel, D.C. As of , FDA records show no recalls naming K972000.

Clearance record

Decision date
Received
(39 days to decision)
Product code
KPR System, X-Ray, Stationary
Regulation
21 CFR 892.1680
Device class
Class II
Review panel
Radiology
Applicant
Ralph Lindel, D.C. 55 Northern Blvd., Suite 410, Great Neck, NY
510(k) summary
Summary
Third party review
No

Clearances, product code KPR

Trailing 12 months
7 clearances under product code KPR in the twelve months to October 2026, August 2026 the highest month at 2.
Show the numbers
Monthly 510(k) clearances under FDA product code KPR, trailing twelve months
MonthClearances
November 20251
December 20250
January 20261
February 20260
March 20260
April 20261
May 20260
June 20261
July 20260
August 20262
September 20261
October 20260