ALKALINE PEPTONE WATER
K-Number: K871640 · 1987-05-13
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Device Summary
Frequently Asked Questions
What is the ALKALINE PEPTONE WATER?
ALKALINE PEPTONE WATER is a medical device that received FDA 510(k) clearance on 1987-05-13. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. The 510(k) number is K871640.
When did ALKALINE PEPTONE WATER receive FDA 510(k) clearance?
ALKALINE PEPTONE WATER received FDA 510(k) clearance on 1987-05-13, under 510(k) number K871640.
Who is the listed applicant for ALKALINE PEPTONE WATER?
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 ALKALINE PEPTONE WATER?
The FDA product code for ALKALINE PEPTONE WATER is JSD.
Related Clinical Trials
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.
Other records listing Bd Becton Dickinson Vacutainer Systems Preanalytic as applicant
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.
Related Devices (Code: JSD)
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.
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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