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FDA 510(k)

MALIS IRRIGATION MODULE 1000

K-Number: K033499 · 2003-11-28

ApplicantValley Forge Scientific Corp.
Decision Date2003-11-28
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MALIS IRRIGATION MODULE 1000 is the device name listed in this FDA 510(k) record. The listed applicant is Valley Forge Scientific Corp.. It received FDA 510(k) clearance on 2003-11-28 under 510(k) number K033499. 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 MALIS IRRIGATION MODULE 1000?

MALIS IRRIGATION MODULE 1000 is a medical device that received FDA 510(k) clearance on 2003-11-28. The listed applicant is Valley Forge Scientific Corp.. The 510(k) number is K033499.

When did MALIS IRRIGATION MODULE 1000 receive FDA 510(k) clearance?

MALIS IRRIGATION MODULE 1000 received FDA 510(k) clearance on 2003-11-28, under 510(k) number K033499.

Who is the listed applicant for MALIS IRRIGATION MODULE 1000?

The FDA 510(k) record lists Valley Forge Scientific Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MALIS IRRIGATION MODULE 1000?

The FDA product code for MALIS IRRIGATION MODULE 1000 is GEI.

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Other records listing Valley Forge Scientific Corp. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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