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FDA 510(k)

FRAMEWAVE WEB

K-Number: K983401 · 1998-12-15

ApplicantMl Strategies, Inc.
Decision Date1998-12-15
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

FRAMEWAVE WEB is the device name listed in this FDA 510(k) record. The listed applicant is Ml Strategies, Inc.. It received FDA 510(k) clearance on 1998-12-15 under 510(k) number K983401. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FRAMEWAVE WEB?

FRAMEWAVE WEB is a medical device that received FDA 510(k) clearance on 1998-12-15. The listed applicant is Ml Strategies, Inc.. The 510(k) number is K983401.

When did FRAMEWAVE WEB receive FDA 510(k) clearance?

FRAMEWAVE WEB received FDA 510(k) clearance on 1998-12-15, under 510(k) number K983401.

Who is the listed applicant for FRAMEWAVE WEB?

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

What is the FDA product code for FRAMEWAVE WEB?

The FDA product code for FRAMEWAVE WEB is LLZ.

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Other records listing Ml Strategies, Inc. as applicant

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Official Source

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