Decision Date1993-12-27
Product CodeDSA
Advisory CommitteeCV
DecisionSubstantially Equivalent
Device Summary
PATIENT CABLE is the device name listed in this FDA 510(k) record. The listed applicant is Sentry Medical Products, Inc.. It received FDA 510(k) clearance on 1993-12-27 under 510(k) number K932704. The device is classified under product code DSA. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the PATIENT CABLE?
PATIENT CABLE is a medical device that received FDA 510(k) clearance on 1993-12-27. The listed applicant is Sentry Medical Products, Inc.. The 510(k) number is K932704.
When did PATIENT CABLE receive FDA 510(k) clearance?
PATIENT CABLE received FDA 510(k) clearance on 1993-12-27, under 510(k) number K932704.
Who is the listed applicant for PATIENT CABLE?
The FDA 510(k) record lists Sentry Medical Products, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PATIENT CABLE?
The FDA product code for PATIENT CABLE is DSA.
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Other records listing Sentry Medical Products, Inc. as applicant
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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.