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FDA 510(k)

INDIPERSE

K-Number: K936113 · 1994-02-10

ApplicantIndisperse Distributing, Inc.
Decision Date1994-02-10
Product CodeEJJ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

INDIPERSE is the device name listed in this FDA 510(k) record. The listed applicant is Indisperse Distributing, Inc.. It received FDA 510(k) clearance on 1994-02-10 under 510(k) number K936113. The device is classified under product code EJJ. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INDIPERSE?

INDIPERSE is a medical device that received FDA 510(k) clearance on 1994-02-10. The listed applicant is Indisperse Distributing, Inc.. The 510(k) number is K936113.

When did INDIPERSE receive FDA 510(k) clearance?

INDIPERSE received FDA 510(k) clearance on 1994-02-10, under 510(k) number K936113.

Who is the listed applicant for INDIPERSE?

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

What is the FDA product code for INDIPERSE?

The FDA product code for INDIPERSE is EJJ.

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Related Devices (Code: EJJ)

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Official Source

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