510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
Medical Device
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K905250Substantially Equivalent

Lobow

Perinatal Systems, Mountain View CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K905250 is the FDA 510(k) clearance record for LOBOW, a class II device, cleared for Perinatal Systems on under FDA product code LIT (Catheter, Angioplasty, Peripheral, Transluminal). FDA records list one 510(k) clearance for Perinatal Systems. As of , FDA records show no recalls naming K905250.

Clearance record

Decision date
Received
(48 days to decision)
Product code
LIT Catheter, Angioplasty, Peripheral, Transluminal
Regulation
21 CFR 870.1250
Device class
Class II
Review panel
Cardiovascular
Applicant
Perinatal Systems 1395 Charleston Rd., Mountain View CA
Third party review
No

Clearances, product code LIT

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