ACS COLLOID OSMOTIC PRESSURE CALIBRATOR
K-Number: K892213 · 1989-06-21
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Device Summary
Frequently Asked Questions
What is the ACS COLLOID OSMOTIC PRESSURE CALIBRATOR?
ACS COLLOID OSMOTIC PRESSURE CALIBRATOR is a medical device that received FDA 510(k) clearance on 1989-06-21. The listed applicant is Analytical Control Systems, Inc.. The 510(k) number is K892213.
When did ACS COLLOID OSMOTIC PRESSURE CALIBRATOR receive FDA 510(k) clearance?
ACS COLLOID OSMOTIC PRESSURE CALIBRATOR received FDA 510(k) clearance on 1989-06-21, under 510(k) number K892213.
Who is the listed applicant for ACS COLLOID OSMOTIC PRESSURE CALIBRATOR?
The FDA 510(k) record lists Analytical Control Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ACS COLLOID OSMOTIC PRESSURE CALIBRATOR?
The FDA product code for ACS COLLOID OSMOTIC PRESSURE CALIBRATOR is JIW.
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 Analytical Control Systems, 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: JIW)
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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