Decision Date1988-06-10
Product CodeBZE
Advisory CommitteeAN
DecisionSubstantially Equivalent
Device Summary
SIMPLEX UNIVERSAL HEATED TUBING SLEEVE is the device name listed in this FDA 510(k) record. The listed applicant is Simplex Medical Corp.. It received FDA 510(k) clearance on 1988-06-10 under 510(k) number K881451. The device is classified under product code BZE. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the SIMPLEX UNIVERSAL HEATED TUBING SLEEVE?
SIMPLEX UNIVERSAL HEATED TUBING SLEEVE is a medical device that received FDA 510(k) clearance on 1988-06-10. The listed applicant is Simplex Medical Corp.. The 510(k) number is K881451.
When did SIMPLEX UNIVERSAL HEATED TUBING SLEEVE receive FDA 510(k) clearance?
SIMPLEX UNIVERSAL HEATED TUBING SLEEVE received FDA 510(k) clearance on 1988-06-10, under 510(k) number K881451.
Who is the listed applicant for SIMPLEX UNIVERSAL HEATED TUBING SLEEVE?
The FDA 510(k) record lists Simplex Medical Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SIMPLEX UNIVERSAL HEATED TUBING SLEEVE?
The FDA product code for SIMPLEX UNIVERSAL HEATED TUBING SLEEVE is BZE.
Related Clinical Trials
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Related Devices (Code: BZE)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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Official Source
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