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FDA 510(k)

MDP DISPOSABLE SYRINGE

K-Number: K890155 · 1989-02-24

ApplicantMediplas Marketing
Decision Date1989-02-24
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MDP DISPOSABLE SYRINGE is the device name listed in this FDA 510(k) record. The listed applicant is Mediplas Marketing. It received FDA 510(k) clearance on 1989-02-24 under 510(k) number K890155. 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 MDP DISPOSABLE SYRINGE?

MDP DISPOSABLE SYRINGE is a medical device that received FDA 510(k) clearance on 1989-02-24. The listed applicant is Mediplas Marketing. The 510(k) number is K890155.

When did MDP DISPOSABLE SYRINGE receive FDA 510(k) clearance?

MDP DISPOSABLE SYRINGE received FDA 510(k) clearance on 1989-02-24, under 510(k) number K890155.

Who is the listed applicant for MDP DISPOSABLE SYRINGE?

The FDA 510(k) record lists Mediplas Marketing as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MDP DISPOSABLE SYRINGE?

The FDA product code for MDP DISPOSABLE SYRINGE is FMF.

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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.

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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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