FDA 510(k)

CARBONACRYL

K-Number: K802976 · 1980-12-19

Decision Date1980-12-19

Product Code

DecisionSubstantially Equivalent

Device Summary

CARBONACRYL is the device name listed in this FDA 510(k) record. The listed applicant is Ipos Luneburg. It received FDA 510(k) clearance on 1980-12-19 under 510(k) number K802976. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CARBONACRYL?

CARBONACRYL is a medical device that received FDA 510(k) clearance on 1980-12-19. The listed applicant is Ipos Luneburg. The 510(k) number is K802976.

When did CARBONACRYL receive FDA 510(k) clearance?

CARBONACRYL received FDA 510(k) clearance on 1980-12-19, under 510(k) number K802976.

Who is the listed applicant for CARBONACRYL?

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

Related Clinical Trials

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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Other records listing Ipos Luneburg as applicant

K834143NYLON COMPRESSION STUMP SHEATH K833868IPOS G.L.P. SYSTEM K831690IPOS ANTI-ADDUCTUS SHOE K802977IPOCARBON STRETCH STOCKINETTE K800749IPOCON 7 K800715OHC DYNAMIC CLUB FOOT BRACE

View all 8 devices →

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.