STERETS INJECTION SWAB
K-Number: K852235 · 1985-06-07
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Device Summary
Frequently Asked Questions
What is the STERETS INJECTION SWAB?
STERETS INJECTION SWAB is a medical device that received FDA 510(k) clearance on 1985-06-07. The listed applicant is Ellis Pharmaceutical Consulting, Inc.. The 510(k) number is K852235.
When did STERETS INJECTION SWAB receive FDA 510(k) clearance?
STERETS INJECTION SWAB received FDA 510(k) clearance on 1985-06-07, under 510(k) number K852235.
Who is the listed applicant for STERETS INJECTION SWAB?
The FDA 510(k) record lists Ellis Pharmaceutical Consulting, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for STERETS INJECTION SWAB?
The FDA product code for STERETS INJECTION SWAB is LKB.
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 Ellis Pharmaceutical Consulting, 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: LKB)
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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