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FDA 510(k)

HEART-CHILL SALINE SLUSH PAD

K-Number: K882035 · 1988-07-28

ApplicantBuckman Co., Inc.
Decision Date1988-07-28
Product CodeDWJ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

HEART-CHILL SALINE SLUSH PAD is the device name listed in this FDA 510(k) record. The listed applicant is Buckman Co., Inc.. It received FDA 510(k) clearance on 1988-07-28 under 510(k) number K882035. 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 HEART-CHILL SALINE SLUSH PAD?

HEART-CHILL SALINE SLUSH PAD is a medical device that received FDA 510(k) clearance on 1988-07-28. The listed applicant is Buckman Co., Inc.. The 510(k) number is K882035.

When did HEART-CHILL SALINE SLUSH PAD receive FDA 510(k) clearance?

HEART-CHILL SALINE SLUSH PAD received FDA 510(k) clearance on 1988-07-28, under 510(k) number K882035.

Who is the listed applicant for HEART-CHILL SALINE SLUSH PAD?

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

What is the FDA product code for HEART-CHILL SALINE SLUSH PAD?

The FDA product code for HEART-CHILL SALINE SLUSH PAD is 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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