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FDA 510(k)

SULLIVAN PASSOVER HUMIDIFER

K-Number: K950582 · 1995-09-15

ApplicantRescare, Inc.
Decision Date1995-09-15
Product CodeBTT
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

SULLIVAN PASSOVER HUMIDIFER is the device name listed in this FDA 510(k) record. The listed applicant is Rescare, Inc.. It received FDA 510(k) clearance on 1995-09-15 under 510(k) number K950582. The device is classified under product code BTT. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SULLIVAN PASSOVER HUMIDIFER?

SULLIVAN PASSOVER HUMIDIFER is a medical device that received FDA 510(k) clearance on 1995-09-15. The listed applicant is Rescare, Inc.. The 510(k) number is K950582.

When did SULLIVAN PASSOVER HUMIDIFER receive FDA 510(k) clearance?

SULLIVAN PASSOVER HUMIDIFER received FDA 510(k) clearance on 1995-09-15, under 510(k) number K950582.

Who is the listed applicant for SULLIVAN PASSOVER HUMIDIFER?

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

What is the FDA product code for SULLIVAN PASSOVER HUMIDIFER?

The FDA product code for SULLIVAN PASSOVER HUMIDIFER is BTT.

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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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