REAGENTS FOR USE ON CONTRAVES DC300, DC500, AL801
K-Number: K873832 · 1987-11-23
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Device Summary
Frequently Asked Questions
What is the REAGENTS FOR USE ON CONTRAVES DC300, DC500, AL801?
REAGENTS FOR USE ON CONTRAVES DC300, DC500, AL801 is a medical device that received FDA 510(k) clearance on 1987-11-23. The listed applicant is In Vitro Diagnostics, Inc.. The 510(k) number is K873832.
When did REAGENTS FOR USE ON CONTRAVES DC300, DC500, AL801 receive FDA 510(k) clearance?
REAGENTS FOR USE ON CONTRAVES DC300, DC500, AL801 received FDA 510(k) clearance on 1987-11-23, under 510(k) number K873832.
Who is the listed applicant for REAGENTS FOR USE ON CONTRAVES DC300, DC500, AL801?
The FDA 510(k) record lists In Vitro Diagnostics, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for REAGENTS FOR USE ON CONTRAVES DC300, DC500, AL801?
The FDA product code for REAGENTS FOR USE ON CONTRAVES DC300, DC500, AL801 is KRZ.
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 In Vitro Diagnostics, 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: KRZ)
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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