RINSE & REFERENCE SOLUTION/BUFFER/LOW & HIGH STAN.
K-Number: K882801 · 1988-08-29
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Device Summary
Frequently Asked Questions
What is the RINSE & REFERENCE SOLUTION/BUFFER/LOW & HIGH STAN.?
RINSE & REFERENCE SOLUTION/BUFFER/LOW & HIGH STAN. is a medical device that received FDA 510(k) clearance on 1988-08-29. The listed applicant is Hf Scientific, Inc.. The 510(k) number is K882801.
When did RINSE & REFERENCE SOLUTION/BUFFER/LOW & HIGH STAN. receive FDA 510(k) clearance?
RINSE & REFERENCE SOLUTION/BUFFER/LOW & HIGH STAN. received FDA 510(k) clearance on 1988-08-29, under 510(k) number K882801.
Who is the listed applicant for RINSE & REFERENCE SOLUTION/BUFFER/LOW & HIGH STAN.?
The FDA 510(k) record lists Hf Scientific, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for RINSE & REFERENCE SOLUTION/BUFFER/LOW & HIGH STAN.?
The FDA product code for RINSE & REFERENCE SOLUTION/BUFFER/LOW & HIGH STAN. is JGS.
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 Hf Scientific, 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: JGS)
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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