ASSURE SELF SEALING STERILIZATION POUCH
K-Number: K933729 · 1994-06-21
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Device Summary
Frequently Asked Questions
What is the ASSURE SELF SEALING STERILIZATION POUCH?
ASSURE SELF SEALING STERILIZATION POUCH is a medical device that received FDA 510(k) clearance on 1994-06-21. The listed applicant is Sultan Chemists, Inc.. The 510(k) number is K933729.
When did ASSURE SELF SEALING STERILIZATION POUCH receive FDA 510(k) clearance?
ASSURE SELF SEALING STERILIZATION POUCH received FDA 510(k) clearance on 1994-06-21, under 510(k) number K933729.
Who is the listed applicant for ASSURE SELF SEALING STERILIZATION POUCH?
The FDA 510(k) record lists Sultan Chemists, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ASSURE SELF SEALING STERILIZATION POUCH?
The FDA product code for ASSURE SELF SEALING STERILIZATION POUCH is KCT.
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 Sultan Chemists, 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: KCT)
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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