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FDA 510(k)

BODY FLUID BARRIER KIT

K-Number: K952961 · 1996-01-23

ApplicantLhb Industries, Inc.
Decision Date1996-01-23
Product CodeFXX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

BODY FLUID BARRIER KIT is the device name listed in this FDA 510(k) record. The listed applicant is Lhb Industries, Inc.. It received FDA 510(k) clearance on 1996-01-23 under 510(k) number K952961. The device is classified under product code FXX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BODY FLUID BARRIER KIT?

BODY FLUID BARRIER KIT is a medical device that received FDA 510(k) clearance on 1996-01-23. The listed applicant is Lhb Industries, Inc.. The 510(k) number is K952961.

When did BODY FLUID BARRIER KIT receive FDA 510(k) clearance?

BODY FLUID BARRIER KIT received FDA 510(k) clearance on 1996-01-23, under 510(k) number K952961.

Who is the listed applicant for BODY FLUID BARRIER KIT?

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

What is the FDA product code for BODY FLUID BARRIER KIT?

The FDA product code for BODY FLUID BARRIER KIT is FXX.

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Related Devices (Code: FXX)

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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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