KENDALL MODEL 6325 SCD SEQUEL COMPRESSION SYSTEM
K-Number: K942664 · 1995-01-17
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Device Summary
Frequently Asked Questions
What is the KENDALL MODEL 6325 SCD SEQUEL COMPRESSION SYSTEM?
KENDALL MODEL 6325 SCD SEQUEL COMPRESSION SYSTEM is a medical device that received FDA 510(k) clearance on 1995-01-17. The listed applicant is The Kendal Co.. The 510(k) number is K942664.
When did KENDALL MODEL 6325 SCD SEQUEL COMPRESSION SYSTEM receive FDA 510(k) clearance?
KENDALL MODEL 6325 SCD SEQUEL COMPRESSION SYSTEM received FDA 510(k) clearance on 1995-01-17, under 510(k) number K942664.
Who is the listed applicant for KENDALL MODEL 6325 SCD SEQUEL COMPRESSION SYSTEM?
The FDA 510(k) record lists The Kendal Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for KENDALL MODEL 6325 SCD SEQUEL COMPRESSION SYSTEM?
The FDA product code for KENDALL MODEL 6325 SCD SEQUEL COMPRESSION SYSTEM is JOW.
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 The Kendal Co. 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: JOW)
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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