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FDA 510(k)

L.A.S.P. LUMBAR AND SACRAL PAD, REPOSITION. SNAP

K-Number: K896936 · 1990-01-22

ApplicantLabeltape Meditect, Inc.
Decision Date1990-01-22
Product CodeGXY
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

L.A.S.P. LUMBAR AND SACRAL PAD, REPOSITION. SNAP is the device name listed in this FDA 510(k) record. The listed applicant is Labeltape Meditect, Inc.. It received FDA 510(k) clearance on 1990-01-22 under 510(k) number K896936. The device is classified under product code GXY. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the L.A.S.P. LUMBAR AND SACRAL PAD, REPOSITION. SNAP?

L.A.S.P. LUMBAR AND SACRAL PAD, REPOSITION. SNAP is a medical device that received FDA 510(k) clearance on 1990-01-22. The listed applicant is Labeltape Meditect, Inc.. The 510(k) number is K896936.

When did L.A.S.P. LUMBAR AND SACRAL PAD, REPOSITION. SNAP receive FDA 510(k) clearance?

L.A.S.P. LUMBAR AND SACRAL PAD, REPOSITION. SNAP received FDA 510(k) clearance on 1990-01-22, under 510(k) number K896936.

Who is the listed applicant for L.A.S.P. LUMBAR AND SACRAL PAD, REPOSITION. SNAP?

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

What is the FDA product code for L.A.S.P. LUMBAR AND SACRAL PAD, REPOSITION. SNAP?

The FDA product code for L.A.S.P. LUMBAR AND SACRAL PAD, REPOSITION. SNAP is GXY.

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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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