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FDA 510(k)

CONSTRUCTA FOAM

K-Number: K820517 · 1982-03-10

ApplicantAlimed, Inc.
Decision Date1982-03-10
Product Code
DecisionSubstantially Equivalent

Device Summary

CONSTRUCTA FOAM is the device name listed in this FDA 510(k) record. The listed applicant is Alimed, Inc.. It received FDA 510(k) clearance on 1982-03-10 under 510(k) number K820517. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CONSTRUCTA FOAM?

CONSTRUCTA FOAM is a medical device that received FDA 510(k) clearance on 1982-03-10. The listed applicant is Alimed, Inc.. The 510(k) number is K820517.

When did CONSTRUCTA FOAM receive FDA 510(k) clearance?

CONSTRUCTA FOAM received FDA 510(k) clearance on 1982-03-10, under 510(k) number K820517.

Who is the listed applicant for CONSTRUCTA FOAM?

The FDA 510(k) record lists Alimed, Inc. 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 Alimed, Inc. 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.

K963527UNIVERSAL ECONO-STRAP, QUALCRAFT UNIVERSAL STRAPSK963528ALIMED POSITIONING 7 SAFETY STRAPS (THREE TYPES), UNIVERSAL CR/MRI WIDE BODY STRAP, UNIVERSAL CT SCANNER STRAP (2 SIZES)K963526STRAP WEDGEK920487MINI VIBRATORK840156PROTECTA COAT SPONGESK822650SUPER DONUT

View all 11 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.

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