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FDA 510(k)

CONTEMPRO2 HOME HEALTH CARE REGULATOR

K-Number: K913327 · 1991-12-20

ApplicantContinental Products, Inc.
Decision Date1991-12-20
Product CodeCAW
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

CONTEMPRO2 HOME HEALTH CARE REGULATOR is the device name listed in this FDA 510(k) record. The listed applicant is Continental Products, Inc.. It received FDA 510(k) clearance on 1991-12-20 under 510(k) number K913327. The device is classified under product code CAW. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CONTEMPRO2 HOME HEALTH CARE REGULATOR?

CONTEMPRO2 HOME HEALTH CARE REGULATOR is a medical device that received FDA 510(k) clearance on 1991-12-20. The listed applicant is Continental Products, Inc.. The 510(k) number is K913327.

When did CONTEMPRO2 HOME HEALTH CARE REGULATOR receive FDA 510(k) clearance?

CONTEMPRO2 HOME HEALTH CARE REGULATOR received FDA 510(k) clearance on 1991-12-20, under 510(k) number K913327.

Who is the listed applicant for CONTEMPRO2 HOME HEALTH CARE REGULATOR?

The FDA 510(k) record lists Continental Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CONTEMPRO2 HOME HEALTH CARE REGULATOR?

The FDA product code for CONTEMPRO2 HOME HEALTH CARE REGULATOR is CAW.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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