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FDA 510(k)

MONOJET 520 20CC SYRINGES W/NEEDLES

K-Number: K822029 · 1982-07-28

Decision Date1982-07-28
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MONOJET 520 20CC SYRINGES W/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 1982-07-28 under 510(k) number K822029. 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 MONOJET 520 20CC SYRINGES W/NEEDLES?

MONOJET 520 20CC SYRINGES W/NEEDLES is a medical device that received FDA 510(k) clearance on 1982-07-28. The listed applicant is Sherwood Medical Co.. The 510(k) number is K822029.

When did MONOJET 520 20CC SYRINGES W/NEEDLES receive FDA 510(k) clearance?

MONOJET 520 20CC SYRINGES W/NEEDLES received FDA 510(k) clearance on 1982-07-28, under 510(k) number K822029.

Who is the listed applicant for MONOJET 520 20CC SYRINGES W/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 MONOJET 520 20CC SYRINGES W/NEEDLES?

The FDA product code for MONOJET 520 20CC SYRINGES W/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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