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FDA 510(k)

MODEL E278OR-ASP SERIES RETRACTABLE

K-Number: K944244 · 1994-11-30

ApplicantValleylab, Inc.
Decision Date1994-11-30
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MODEL E278OR-ASP SERIES RETRACTABLE is the device name listed in this FDA 510(k) record. The listed applicant is Valleylab, Inc.. It received FDA 510(k) clearance on 1994-11-30 under 510(k) number K944244. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL E278OR-ASP SERIES RETRACTABLE?

MODEL E278OR-ASP SERIES RETRACTABLE is a medical device that received FDA 510(k) clearance on 1994-11-30. The listed applicant is Valleylab, Inc.. The 510(k) number is K944244.

When did MODEL E278OR-ASP SERIES RETRACTABLE receive FDA 510(k) clearance?

MODEL E278OR-ASP SERIES RETRACTABLE received FDA 510(k) clearance on 1994-11-30, under 510(k) number K944244.

Who is the listed applicant for MODEL E278OR-ASP SERIES RETRACTABLE?

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

What is the FDA product code for MODEL E278OR-ASP SERIES RETRACTABLE?

The FDA product code for MODEL E278OR-ASP SERIES RETRACTABLE is GEI.

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Related Devices (Code: GEI)

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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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