510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K030520Substantially Equivalent

Intera Family

Philips North America LLC, Bothell WA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K030520 is the FDA 510(k) clearance record for INTERA FAMILY, a class II device, cleared for Philips Medical Systems North America Co. on under FDA product code LNH (System, Nuclear Magnetic Resonance Imaging). FDA records list 680 510(k) clearances for Philips North America LLC, from to . As of , FDA records show 11 recalls naming K030520.

Clearance record

Decision date
Received
(15 days to decision)
Product code
LNH System, Nuclear Magnetic Resonance Imaging
Regulation
21 CFR 892.1000
Device class
Class II
Review panel
Radiology
Applicant
Philips Medical Systems North America Co. 22100 Bothell Everett Hwy., Bothell WA
510(k) summary
Summary PDF
Third party review
Yes

Clearances, product code LNH

Trailing 12 months
25 clearances under product code LNH in the twelve months to October 2026, March 2026 the highest month at 6.
Show the numbers
Monthly 510(k) clearances under FDA product code LNH, trailing twelve months
MonthClearances
November 20251
December 20253
January 20261
February 20264
March 20266
April 20261
May 20261
June 20260
July 20262
August 20263
September 20263
October 20260