MONOJECT STERILE 1/2 CC & 1CC SYRINGES W & W/O NEE
K-Number: K851090 · 1985-04-12
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Device Summary
Frequently Asked Questions
What is the MONOJECT STERILE 1/2 CC & 1CC SYRINGES W & W/O NEE?
MONOJECT STERILE 1/2 CC & 1CC SYRINGES W & W/O NEE is a medical device that received FDA 510(k) clearance on 1985-04-12. The listed applicant is Sherwood Medical Co.. The 510(k) number is K851090.
When did MONOJECT STERILE 1/2 CC & 1CC SYRINGES W & W/O NEE receive FDA 510(k) clearance?
MONOJECT STERILE 1/2 CC & 1CC SYRINGES W & W/O NEE received FDA 510(k) clearance on 1985-04-12, under 510(k) number K851090.
Who is the listed applicant for MONOJECT STERILE 1/2 CC & 1CC SYRINGES W & W/O NEE?
The FDA 510(k) record lists Sherwood Medical Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MONOJECT STERILE 1/2 CC & 1CC SYRINGES W & W/O NEE?
The FDA product code for MONOJECT STERILE 1/2 CC & 1CC SYRINGES W & W/O NEE is FMF.
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 Sherwood Medical 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: FMF)
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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