DADE LOW IONIC STRENGTH SOLUITION (LISS)
K-Number: K790776 · 1979-05-23
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Device Summary
Frequently Asked Questions
What is the DADE LOW IONIC STRENGTH SOLUITION (LISS)?
DADE LOW IONIC STRENGTH SOLUITION (LISS) is a medical device that received FDA 510(k) clearance on 1979-05-23. The listed applicant is Dade, Baxter Travenol Diagnostics, Inc.. The 510(k) number is K790776.
When did DADE LOW IONIC STRENGTH SOLUITION (LISS) receive FDA 510(k) clearance?
DADE LOW IONIC STRENGTH SOLUITION (LISS) received FDA 510(k) clearance on 1979-05-23, under 510(k) number K790776.
Who is the listed applicant for DADE LOW IONIC STRENGTH SOLUITION (LISS)?
The FDA 510(k) record lists Dade, Baxter Travenol Diagnostics, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DADE LOW IONIC STRENGTH SOLUITION (LISS)?
The FDA product code for DADE LOW IONIC STRENGTH SOLUITION (LISS) is KSG.
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 Dade, Baxter Travenol 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: KSG)
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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