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FDA 510(k)

WARMTOUCH CARDIAC BLANKET,CATALOG # 503-0860

K-Number: K014121 · 2002-01-11

ApplicantNellcor Puritan Bennett, Inc.
Decision Date2002-01-11
Product CodeDWJ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

WARMTOUCH CARDIAC BLANKET,CATALOG # 503-0860 is the device name listed in this FDA 510(k) record. The listed applicant is Nellcor Puritan Bennett, Inc.. It received FDA 510(k) clearance on 2002-01-11 under 510(k) number K014121. The device is classified under product code DWJ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WARMTOUCH CARDIAC BLANKET,CATALOG # 503-0860?

WARMTOUCH CARDIAC BLANKET,CATALOG # 503-0860 is a medical device that received FDA 510(k) clearance on 2002-01-11. The listed applicant is Nellcor Puritan Bennett, Inc.. The 510(k) number is K014121.

When did WARMTOUCH CARDIAC BLANKET,CATALOG # 503-0860 receive FDA 510(k) clearance?

WARMTOUCH CARDIAC BLANKET,CATALOG # 503-0860 received FDA 510(k) clearance on 2002-01-11, under 510(k) number K014121.

Who is the listed applicant for WARMTOUCH CARDIAC BLANKET,CATALOG # 503-0860?

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

What is the FDA product code for WARMTOUCH CARDIAC BLANKET,CATALOG # 503-0860?

The FDA product code for WARMTOUCH CARDIAC BLANKET,CATALOG # 503-0860 is DWJ.

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Related Devices (Code: DWJ)

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Official Source

View on FDA Database →

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

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