ClearanceBrief
Company ยท US

H & P Industries, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 1983 to 1990. Name variants (Inc, Corp, punctuation) are merged.

5510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
GECBrush, Scrub, Operating-Room2
JOTElectrode, Gel, Electrosurgical1
KMJLubricant, Patient1
LKBPad, Alcohol, Device Disinfectant1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Jun 22, 1990K901217TRIA-SONIC ULTRA SOUND TRANSMISSION GEL
H & P Industries, Inc.
JOT
Apr 1, 1987K871169LUBRICATING JELLY
H & P Industries, Inc.
KMJ
Apr 9, 1986K860961GAMMA RADIATION STERILIZED ALCOHOL PREP PADS
H & P Industries, Inc.
LKB
Apr 6, 1983K830394PROVIDONE-IODINE PREP-PADS & TOWELETTES
H & P Industries, Inc.
GEC
Apr 6, 1983K830393PROVIDONE-IODINE SWABSTICKS
H & P Industries, Inc.
GEC

Latest recalls

DateFirm and productCodeLinked 510(k)
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