CELL-DYN DIFF. SCREEN ISOTONIC DILUENT
K-Number: K873347 · 1987-09-09
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Device Summary
Frequently Asked Questions
What is the CELL-DYN DIFF. SCREEN ISOTONIC DILUENT?
CELL-DYN DIFF. SCREEN ISOTONIC DILUENT is a medical device that received FDA 510(k) clearance on 1987-09-09. The listed applicant is Abbott Diagnostics. The 510(k) number is K873347.
When did CELL-DYN DIFF. SCREEN ISOTONIC DILUENT receive FDA 510(k) clearance?
CELL-DYN DIFF. SCREEN ISOTONIC DILUENT received FDA 510(k) clearance on 1987-09-09, under 510(k) number K873347.
Who is the listed applicant for CELL-DYN DIFF. SCREEN ISOTONIC DILUENT?
The FDA 510(k) record lists Abbott Diagnostics as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CELL-DYN DIFF. SCREEN ISOTONIC DILUENT?
The FDA product code for CELL-DYN DIFF. SCREEN ISOTONIC DILUENT is GIF.
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 Abbott Diagnostics 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: GIF)
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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