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FDA 510(k)

LOKSHOT PISTON SYRINGE

K-Number: K891467 · 1989-05-24

ApplicantFlp Ent., Inc.
Decision Date1989-05-24
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

LOKSHOT PISTON SYRINGE is the device name listed in this FDA 510(k) record. The listed applicant is Flp Ent., Inc.. It received FDA 510(k) clearance on 1989-05-24 under 510(k) number K891467. 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 LOKSHOT PISTON SYRINGE?

LOKSHOT PISTON SYRINGE is a medical device that received FDA 510(k) clearance on 1989-05-24. The listed applicant is Flp Ent., Inc.. The 510(k) number is K891467.

When did LOKSHOT PISTON SYRINGE receive FDA 510(k) clearance?

LOKSHOT PISTON SYRINGE received FDA 510(k) clearance on 1989-05-24, under 510(k) number K891467.

Who is the listed applicant for LOKSHOT PISTON SYRINGE?

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

What is the FDA product code for LOKSHOT PISTON SYRINGE?

The FDA product code for LOKSHOT PISTON SYRINGE is FMF.

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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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