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FDA 510(k)

MONOJECT STERILE 6CC SYRINGE W/ & WO/ NEEDLES

K-Number: K852588 · 1985-07-23

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

Device Summary

MONOJECT STERILE 6CC SYRINGE W/ & WO/ NEEDLES 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 K852588. 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 6CC SYRINGE W/ & WO/ NEEDLES?

MONOJECT STERILE 6CC SYRINGE W/ & WO/ NEEDLES 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 K852588.

When did MONOJECT STERILE 6CC SYRINGE W/ & WO/ NEEDLES receive FDA 510(k) clearance?

MONOJECT STERILE 6CC SYRINGE W/ & WO/ NEEDLES received FDA 510(k) clearance on 1985-07-23, under 510(k) number K852588.

Who is the listed applicant for MONOJECT STERILE 6CC SYRINGE W/ & WO/ NEEDLES?

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 6CC SYRINGE W/ & WO/ NEEDLES?

The FDA product code for MONOJECT STERILE 6CC SYRINGE W/ & WO/ NEEDLES 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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