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FDA 510(k)

MONOJECT STERILE 1/2 CC & 1CC SYRINGES W & W/O NEE

K-Number: K851090 · 1985-04-12

Decision Date1985-04-12
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MONOJECT STERILE 1/2 CC & 1CC SYRINGES W & W/O NEE is the device name listed in this FDA 510(k) record. The listed applicant is Sherwood Medical Co.. It received FDA 510(k) clearance on 1985-04-12 under 510(k) number K851090. The device is classified under product code FMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 191 devices →

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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