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FDA 510(k)

SLICES

K-Number: K941812 · 1994-08-12

ApplicantMicrosignal Corp.
Decision Date1994-08-12
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SLICES is the device name listed in this FDA 510(k) record. The listed applicant is Microsignal Corp.. It received FDA 510(k) clearance on 1994-08-12 under 510(k) number K941812. The device is classified under product code LNH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SLICES?

SLICES is a medical device that received FDA 510(k) clearance on 1994-08-12. The listed applicant is Microsignal Corp.. The 510(k) number is K941812.

When did SLICES receive FDA 510(k) clearance?

SLICES received FDA 510(k) clearance on 1994-08-12, under 510(k) number K941812.

Who is the listed applicant for SLICES?

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

What is the FDA product code for SLICES?

The FDA product code for SLICES is LNH.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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