SENTINEL CHOLINESTERASE LIQUID MODEL NUMBER 17.019A & 17.606
K-Number: K981800 · 1998-07-06
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Device Summary
Frequently Asked Questions
What is the SENTINEL CHOLINESTERASE LIQUID MODEL NUMBER 17.019A & 17.606?
SENTINEL CHOLINESTERASE LIQUID MODEL NUMBER 17.019A & 17.606 is a medical device that received FDA 510(k) clearance on 1998-07-06. The listed applicant is Equal Diagnostics, Inc.. The 510(k) number is K981800.
When did SENTINEL CHOLINESTERASE LIQUID MODEL NUMBER 17.019A & 17.606 receive FDA 510(k) clearance?
SENTINEL CHOLINESTERASE LIQUID MODEL NUMBER 17.019A & 17.606 received FDA 510(k) clearance on 1998-07-06, under 510(k) number K981800.
Who is the listed applicant for SENTINEL CHOLINESTERASE LIQUID MODEL NUMBER 17.019A & 17.606?
The FDA 510(k) record lists Equal Diagnostics, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SENTINEL CHOLINESTERASE LIQUID MODEL NUMBER 17.019A & 17.606?
The FDA product code for SENTINEL CHOLINESTERASE LIQUID MODEL NUMBER 17.019A & 17.606 is HIH.
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 Equal Diagnostics, Inc. 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: HIH)
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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