IMSI, VITAL CALL
K-Number: K873612 · 1987-11-23
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Device Summary
Frequently Asked Questions
What is the IMSI, VITAL CALL?
IMSI, VITAL CALL is a medical device that received FDA 510(k) clearance on 1987-11-23. The listed applicant is Intl. Management Services, Inc.. The 510(k) number is K873612.
When did IMSI, VITAL CALL receive FDA 510(k) clearance?
IMSI, VITAL CALL received FDA 510(k) clearance on 1987-11-23, under 510(k) number K873612.
Who is the listed applicant for IMSI, VITAL CALL?
The FDA 510(k) record lists Intl. Management Services, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for IMSI, VITAL CALL?
The FDA product code for IMSI, VITAL CALL is IQA.
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 Intl. Management Services, 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: IQA)
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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