PRIMUS PSS SERIES STERILIZERS
K-Number: K926185 · 1994-05-09
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Device Summary
Frequently Asked Questions
What is the PRIMUS PSS SERIES STERILIZERS?
PRIMUS PSS SERIES STERILIZERS is a medical device that received FDA 510(k) clearance on 1994-05-09. The listed applicant is Primus Sterilizer Co., Inc.. The 510(k) number is K926185.
When did PRIMUS PSS SERIES STERILIZERS receive FDA 510(k) clearance?
PRIMUS PSS SERIES STERILIZERS received FDA 510(k) clearance on 1994-05-09, under 510(k) number K926185.
Who is the listed applicant for PRIMUS PSS SERIES STERILIZERS?
The FDA 510(k) record lists Primus Sterilizer Co., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PRIMUS PSS SERIES STERILIZERS?
The FDA product code for PRIMUS PSS SERIES STERILIZERS is FLE.
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 Primus Sterilizer Co., 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: FLE)
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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