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FDA 510(k)

MONOJECT STERILE 60CC SYRINGES

K-Number: K852580 · 1985-07-23

Decision Date1985-07-23
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MONOJECT STERILE 60CC SYRINGES 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 1985-07-23 under 510(k) number K852580. 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 60CC SYRINGES?

MONOJECT STERILE 60CC SYRINGES is a medical device that received FDA 510(k) clearance on 1985-07-23. The listed applicant is Sherwood Medical Co.. The 510(k) number is K852580.

When did MONOJECT STERILE 60CC SYRINGES receive FDA 510(k) clearance?

MONOJECT STERILE 60CC SYRINGES received FDA 510(k) clearance on 1985-07-23, under 510(k) number K852580.

Who is the listed applicant for MONOJECT STERILE 60CC SYRINGES?

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 60CC SYRINGES?

The FDA product code for MONOJECT STERILE 60CC SYRINGES 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

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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