PM3300 INTERMITTENT VACUUM

Regulator, Vacuum

PRECISION MEDICAL, INC.

The following data is part of a premarket notification filed by Precision Medical, Inc. with the FDA for Pm3300 Intermittent Vacuum.

Pre-market Notification Details

Device IDK944479
510k NumberK944479
Device Name:PM3300 INTERMITTENT VACUUM
ClassificationRegulator, Vacuum
Applicant PRECISION MEDICAL, INC. 300 HELD DR. Northampton,  PA  18067
ContactMichael A Krupa
CorrespondentMichael A Krupa
PRECISION MEDICAL, INC. 300 HELD DR. Northampton,  PA  18067
Product CodeKDP  
CFR Regulation Number880.6740 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1994-09-13
Decision Date1994-12-22

NIH GUDID Devices

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