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FDA 510(k)

GI MOTILITY TEST MEDIUM W/TTC

K-Number: K863603 · 1986-09-30

ApplicantBd Becton Dickinson Vacutainer Systems Preanalytic
Decision Date1986-09-30
Product CodeJSS
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

GI MOTILITY TEST MEDIUM W/TTC is the device name listed in this FDA 510(k) record. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. It received FDA 510(k) clearance on 1986-09-30 under 510(k) number K863603. The device is classified under product code JSS. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GI MOTILITY TEST MEDIUM W/TTC?

GI MOTILITY TEST MEDIUM W/TTC is a medical device that received FDA 510(k) clearance on 1986-09-30. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. The 510(k) number is K863603.

When did GI MOTILITY TEST MEDIUM W/TTC receive FDA 510(k) clearance?

GI MOTILITY TEST MEDIUM W/TTC received FDA 510(k) clearance on 1986-09-30, under 510(k) number K863603.

Who is the listed applicant for GI MOTILITY TEST MEDIUM W/TTC?

The FDA 510(k) record lists Bd Becton Dickinson Vacutainer Systems Preanalytic as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for GI MOTILITY TEST MEDIUM W/TTC?

The FDA product code for GI MOTILITY TEST MEDIUM W/TTC is JSS.

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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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