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FDA 510(k)

LACTOSORB SHEETS

K-Number: K992158 · 1999-08-20

ApplicantBiomet, Inc.
Decision Date1999-08-20
Product CodeJEY
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

LACTOSORB SHEETS is the device name listed in this FDA 510(k) record. The listed applicant is Biomet, Inc.. It received FDA 510(k) clearance on 1999-08-20 under 510(k) number K992158. 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 SHEETS?

LACTOSORB SHEETS is a medical device that received FDA 510(k) clearance on 1999-08-20. The listed applicant is Biomet, Inc.. The 510(k) number is K992158.

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

LACTOSORB SHEETS received FDA 510(k) clearance on 1999-08-20, under 510(k) number K992158.

Who is the listed applicant for LACTOSORB SHEETS?

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 SHEETS?

The FDA product code for LACTOSORB SHEETS is 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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