Q4.5-5.0PB-4.5
K-Number: K951342 · 1995-04-25
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Device Summary
Frequently Asked Questions
What is the Q4.5-5.0PB-4.5?
Q4.5-5.0PB-4.5 is a medical device that received FDA 510(k) clearance on 1995-04-25. The listed applicant is Central Solutions, Inc.. The 510(k) number is K951342.
When did Q4.5-5.0PB-4.5 receive FDA 510(k) clearance?
Q4.5-5.0PB-4.5 received FDA 510(k) clearance on 1995-04-25, under 510(k) number K951342.
Who is the listed applicant for Q4.5-5.0PB-4.5?
The FDA 510(k) record lists Central Solutions, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Q4.5-5.0PB-4.5?
The FDA product code for Q4.5-5.0PB-4.5 is LRJ. This falls under the Clinical Lab category.
Other records listing Central Solutions, 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: LRJ)
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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