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FDA 510(k)

NYLON COMPRESSION STUMP SHEATH

K-Number: K834143 · 1984-01-09

ApplicantIpos Luneburg
Decision Date1984-01-09
Product Code
DecisionSubstantially Equivalent

Device Summary

NYLON COMPRESSION STUMP SHEATH is the device name listed in this FDA 510(k) record. The listed applicant is Ipos Luneburg. It received FDA 510(k) clearance on 1984-01-09 under 510(k) number K834143. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NYLON COMPRESSION STUMP SHEATH?

NYLON COMPRESSION STUMP SHEATH is a medical device that received FDA 510(k) clearance on 1984-01-09. The listed applicant is Ipos Luneburg. The 510(k) number is K834143.

When did NYLON COMPRESSION STUMP SHEATH receive FDA 510(k) clearance?

NYLON COMPRESSION STUMP SHEATH received FDA 510(k) clearance on 1984-01-09, under 510(k) number K834143.

Who is the listed applicant for NYLON COMPRESSION STUMP SHEATH?

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

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Other records listing Ipos Luneburg 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.

K833868IPOS G.L.P. SYSTEMK831690IPOS ANTI-ADDUCTUS SHOEK802976CARBONACRYLK802977IPOCARBON STRETCH STOCKINETTEK800749IPOCON 7K800716ORTHOTIC LEG GAIT CORRECTOR DEVICE

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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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