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Pro-Tech, Inc.

FDA Regulatory Profile

Pro-Tech, Inc. has 0 FDA recalls, 0 inspections, 7 510(k) clearances and 1 compliance action on record.

Latest 510(k)
May 4, 1995

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Nov 8, 2026File dated Nov 3, 2026Current
510(k) clearances7Nov 8, 2026File dated Nov 2, 2026Current
Inspections0Nov 11, 2026Newest record Nov 5, 2026Current
Compliance actions1Nov 2, 2026Newest record Oct 29, 2026Current

Related names

NameRecalls510(k)InspectionsComplianceMost recent recall
Pro-Tech Design And Manufacturing
Same company group		0060—
Pro-Tech Design And Mfg
Same company group		0050—
Protech
Same company group		0100—

Recent 510(k) Clearances

K-NumberDeviceDate
K940013BODY POSITION INDICATOR, MODEL BPI1May 4, 1995
K940015SNORING MICROPHONE, SM1Jan 11, 1995
K940014PLM SENSOR, MODEL PLM1Nov 10, 1994
K924752FREEDOM OXIMETER/EEG DIGITAL INTERFACESep 10, 1993
K923402CRYSTAL TRACE PIEZO RESPIRATORY EFFORT SENSORDec 30, 1992
K913396CANNULA STYLE THERMOCOUPLESMay 22, 1992
K913395EZ-1 SYSTEM RESPIRATORY EFFORT SENSORSMay 20, 1992

FDA data resources

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.