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FDA 510(k)

CONTRASYL IMPRESSION MATERIAL

K-Number: K870011 · 1987-03-19

ApplicantContracap
Decision Date1987-03-19
Product CodeELW
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

CONTRASYL IMPRESSION MATERIAL is the device name listed in this FDA 510(k) record. The listed applicant is Contracap. It received FDA 510(k) clearance on 1987-03-19 under 510(k) number K870011. The device is classified under product code ELW. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CONTRASYL IMPRESSION MATERIAL?

CONTRASYL IMPRESSION MATERIAL is a medical device that received FDA 510(k) clearance on 1987-03-19. The listed applicant is Contracap. The 510(k) number is K870011.

When did CONTRASYL IMPRESSION MATERIAL receive FDA 510(k) clearance?

CONTRASYL IMPRESSION MATERIAL received FDA 510(k) clearance on 1987-03-19, under 510(k) number K870011.

Who is the listed applicant for CONTRASYL IMPRESSION MATERIAL?

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

What is the FDA product code for CONTRASYL IMPRESSION MATERIAL?

The FDA product code for CONTRASYL IMPRESSION MATERIAL is ELW.

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Related Devices (Code: ELW)

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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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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