510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K972158Substantially Equivalent

Go Medical Patient Controlled Analgesia Devices

Princeton Regulatory Assoc., Princeton NJ / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K972158 is the FDA 510(k) clearance record for GO MEDICAL PATIENT CONTROLLED ANALGESIA DEVICES, a class II device, cleared for Princeton Regulatory Assoc. on under FDA product code MEB (Pump, Infusion, Elastomeric). FDA records list 4 510(k) clearances for Princeton Regulatory Assoc., from to . As of , FDA records show no recalls naming K972158.

Clearance record

Decision date
Received
(256 days to decision)
Product code
MEB Pump, Infusion, Elastomeric
Regulation
21 CFR 880.5725
Device class
Class II
Review panel
General Hospital
Applicant
Princeton Regulatory Assoc. 116 Village Blvd., Suite 200, Princeton NJ
510(k) summary
Statement
Third party review
No

Clearances, product code MEB

Trailing 12 months
1 clearance under product code MEB in the twelve months to October 2026, April 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code MEB, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20261
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260