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FDA 510(k)

LACTOSORB RAPIDFLAP

K-Number: K003281 · 2001-08-07

ApplicantBiomet, Inc.
Decision Date2001-08-07
Product CodeJEY
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

LACTOSORB RAPIDFLAP is the device name listed in this FDA 510(k) record. The listed applicant is Biomet, Inc.. It received FDA 510(k) clearance on 2001-08-07 under 510(k) number K003281. The device is classified under product code JEY. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LACTOSORB RAPIDFLAP?

LACTOSORB RAPIDFLAP is a medical device that received FDA 510(k) clearance on 2001-08-07. The listed applicant is Biomet, Inc.. The 510(k) number is K003281.

When did LACTOSORB RAPIDFLAP receive FDA 510(k) clearance?

LACTOSORB RAPIDFLAP received FDA 510(k) clearance on 2001-08-07, under 510(k) number K003281.

Who is the listed applicant for LACTOSORB RAPIDFLAP?

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

What is the FDA product code for LACTOSORB RAPIDFLAP?

The FDA product code for LACTOSORB RAPIDFLAP is JEY.

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Related Devices (Code: JEY)

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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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