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FDA 510(k)

LITE-TOUCH SYRINGE

K-Number: K983430 · 1999-02-09

ApplicantMedicore, Inc.
Decision Date1999-02-09
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

LITE-TOUCH SYRINGE is the device name listed in this FDA 510(k) record. The listed applicant is Medicore, Inc.. It received FDA 510(k) clearance on 1999-02-09 under 510(k) number K983430. 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 LITE-TOUCH SYRINGE?

LITE-TOUCH SYRINGE is a medical device that received FDA 510(k) clearance on 1999-02-09. The listed applicant is Medicore, Inc.. The 510(k) number is K983430.

When did LITE-TOUCH SYRINGE receive FDA 510(k) clearance?

LITE-TOUCH SYRINGE received FDA 510(k) clearance on 1999-02-09, under 510(k) number K983430.

Who is the listed applicant for LITE-TOUCH SYRINGE?

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

What is the FDA product code for LITE-TOUCH SYRINGE?

The FDA product code for LITE-TOUCH SYRINGE is FMF.

Related Clinical Trials

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Other records listing Medicore, Inc. 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.

K880869MEDI-LETK810681MEDI-LANCE

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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