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FDA 510(k)

TERUMO DISPOSABLE HYPODERMC SYRINGE

K-Number: K980181 · 1998-04-02

ApplicantTerumo Medical Corp.
Decision Date1998-04-02
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

TERUMO DISPOSABLE HYPODERMC SYRINGE is the device name listed in this FDA 510(k) record. The listed applicant is Terumo Medical Corp.. It received FDA 510(k) clearance on 1998-04-02 under 510(k) number K980181. 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 TERUMO DISPOSABLE HYPODERMC SYRINGE?

TERUMO DISPOSABLE HYPODERMC SYRINGE is a medical device that received FDA 510(k) clearance on 1998-04-02. The listed applicant is Terumo Medical Corp.. The 510(k) number is K980181.

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

TERUMO DISPOSABLE HYPODERMC SYRINGE received FDA 510(k) clearance on 1998-04-02, under 510(k) number K980181.

Who is the listed applicant for TERUMO DISPOSABLE HYPODERMC SYRINGE?

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

What is the FDA product code for TERUMO DISPOSABLE HYPODERMC SYRINGE?

The FDA product code for TERUMO DISPOSABLE HYPODERMC SYRINGE is FMF.

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Other records listing Terumo Medical Corp. as applicant

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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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