KEMTROL SERUM CONTROL-ABNORMAL
K-Number: K920926 · 1992-05-07
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Device Summary
Frequently Asked Questions
What is the KEMTROL SERUM CONTROL-ABNORMAL?
KEMTROL SERUM CONTROL-ABNORMAL is a medical device that received FDA 510(k) clearance on 1992-05-07. The listed applicant is Helena Laboratories. The 510(k) number is K920926.
When did KEMTROL SERUM CONTROL-ABNORMAL receive FDA 510(k) clearance?
KEMTROL SERUM CONTROL-ABNORMAL received FDA 510(k) clearance on 1992-05-07, under 510(k) number K920926.
Who is the listed applicant for KEMTROL SERUM CONTROL-ABNORMAL?
The FDA 510(k) record lists Helena Laboratories as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for KEMTROL SERUM CONTROL-ABNORMAL?
The FDA product code for KEMTROL SERUM CONTROL-ABNORMAL is JJY.
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 Helena Laboratories 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: JJY)
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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