Shenzhen Pango Electronic Co., Ltd.

FDA Regulatory Profile

Shenzhen Pango Electronic Co., Ltd. has 0 FDA recalls, 1 inspection, 9 510(k) clearances and 0 compliance actions on record.

Latest inspection
Nov 13, 2014 · NAI
Latest 510(k)
Nov 10, 2021

Reviewing Shenzhen Pango Electronic Co., Ltd. as a supplier? Request a free FDA snapshot: name up to five suppliers and get a PDF of their public FDA record, with sources and dates. You do not need an API connection. Each snapshot is prepared by hand.

Request a free FDA snapshot

Or get Shenzhen Pango Electronic Co., Ltd.'s full FDA risk summary, with inspections, warning letters, Form 483s and import alerts by site, in Claude, Cursor or ChatGPT.

Get a free API key

Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Oct 23, 2026Not statedCurrent
510(k) clearances9Oct 4, 2026Not statedCurrent
Inspections1Oct 23, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent FDA Inspections

DateSiteProductClassificationFEI
Nov 13, 2014Shenzhen, ChinaDevicesNo Action Indicated (NAI)3006792041

NAI means no objectionable conditions or practices were found during the inspection. VAI means objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action. OAI means regulatory and/or administrative actions are recommended.

Recent 510(k) Clearances

K-NumberDeviceDate
K203746Venen-trainer (Model: FM150, SFM90)Nov 10, 2021
K200716Electronic Blood Pressure MonitorDec 4, 2020
K182597Infrared thermometerApr 3, 2019
K170151Electronic Blood Pressure MonitorOct 13, 2017
K161845Electronic Blood Pressure MonitorJul 31, 2017
K131558PG-800B SERIES, INCLUDING PG-800BD, PG-800B-1, PG-800BD-1, PG-800B3, PG-800B4, PG-800B4D, PG-800B5…Aug 30, 2013
K131569PG-800A SERIESJun 14, 2013
K102988ELECTRONIC BLOOD PRESURE MONITORNov 9, 2010
K102920ELECTRONIC BLOOD PRESSURE MONITOROct 15, 2010