MODULUS VERNI-TROL ANESTHETIC VAPORIZER

Vaporizer, Anesthesia, Non-heated

OHIO MEDICAL PRODUCTS

The following data is part of a premarket notification filed by Ohio Medical Products with the FDA for Modulus Verni-trol Anesthetic Vaporizer.

Pre-market Notification Details

Device IDK821966
510k NumberK821966
Device Name:MODULUS VERNI-TROL ANESTHETIC VAPORIZER
ClassificationVaporizer, Anesthesia, Non-heated
Applicant OHIO MEDICAL PRODUCTS 803 N. Front St. Suite 3 Mchenry,  IL  60050
Product CodeCAD  
CFR Regulation Number868.5880 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1982-07-02
Decision Date1982-07-16

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