EMDS SALICYLATE (SAL) CALIBRATOR, NO# 67641/93
K-Number: K872321 · 1987-08-28
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Device Summary
Frequently Asked Questions
What is the EMDS SALICYLATE (SAL) CALIBRATOR, NO# 67641/93?
EMDS SALICYLATE (SAL) CALIBRATOR, NO# 67641/93 is a medical device that received FDA 510(k) clearance on 1987-08-28. The listed applicant is Em Diagnostic Systems, Inc.. The 510(k) number is K872321.
When did EMDS SALICYLATE (SAL) CALIBRATOR, NO# 67641/93 receive FDA 510(k) clearance?
EMDS SALICYLATE (SAL) CALIBRATOR, NO# 67641/93 received FDA 510(k) clearance on 1987-08-28, under 510(k) number K872321.
Who is the listed applicant for EMDS SALICYLATE (SAL) CALIBRATOR, NO# 67641/93?
The FDA 510(k) record lists Em Diagnostic Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for EMDS SALICYLATE (SAL) CALIBRATOR, NO# 67641/93?
The FDA product code for EMDS SALICYLATE (SAL) CALIBRATOR, NO# 67641/93 is DKJ.
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 Em Diagnostic 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: DKJ)
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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