BEDPAN, GENERAL MEDICAL MEDI-PAK

Bedpan

LANDMARK PLASTICS

The following data is part of a premarket notification filed by Landmark Plastics with the FDA for Bedpan, General Medical Medi-pak.

Pre-market Notification Details

Device IDK760490
510k NumberK760490
Device Name:BEDPAN, GENERAL MEDICAL MEDI-PAK
ClassificationBedpan
Applicant LANDMARK PLASTICS 803 N. Front St. Suite 3 Mchenry,  IL  60050
Product CodeFOB  
CFR Regulation Number880.6730 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1976-08-23
Decision Date1976-11-12

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