HEMATRAK MATURITY PROFILE OPTION
K-Number: K761208 · 1977-02-28
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Device Summary
Frequently Asked Questions
What is the HEMATRAK MATURITY PROFILE OPTION?
HEMATRAK MATURITY PROFILE OPTION is a medical device that received FDA 510(k) clearance on 1977-02-28. The listed applicant is Geometric Data, Div. Smithkline Corp.. The 510(k) number is K761208.
When did HEMATRAK MATURITY PROFILE OPTION receive FDA 510(k) clearance?
HEMATRAK MATURITY PROFILE OPTION received FDA 510(k) clearance on 1977-02-28, under 510(k) number K761208.
Who is the listed applicant for HEMATRAK MATURITY PROFILE OPTION?
The FDA 510(k) record lists Geometric Data, Div. Smithkline Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for HEMATRAK MATURITY PROFILE OPTION?
The FDA product code for HEMATRAK MATURITY PROFILE OPTION is GKZ.
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 Geometric Data, Div. Smithkline Corp. 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: GKZ)
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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