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FDA 510(k)

VINYL POLYSILOXANE 2 COMPONENT VULCANIZING SYSTEM

K-Number: K930248 · 1994-01-07

Decision Date1994-01-07
Product CodeELW
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

VINYL POLYSILOXANE 2 COMPONENT VULCANIZING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Crown Delta Corp.. It received FDA 510(k) clearance on 1994-01-07 under 510(k) number K930248. 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 VINYL POLYSILOXANE 2 COMPONENT VULCANIZING SYSTEM?

VINYL POLYSILOXANE 2 COMPONENT VULCANIZING SYSTEM is a medical device that received FDA 510(k) clearance on 1994-01-07. The listed applicant is Crown Delta Corp.. The 510(k) number is K930248.

When did VINYL POLYSILOXANE 2 COMPONENT VULCANIZING SYSTEM receive FDA 510(k) clearance?

VINYL POLYSILOXANE 2 COMPONENT VULCANIZING SYSTEM received FDA 510(k) clearance on 1994-01-07, under 510(k) number K930248.

Who is the listed applicant for VINYL POLYSILOXANE 2 COMPONENT VULCANIZING SYSTEM?

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

What is the FDA product code for VINYL POLYSILOXANE 2 COMPONENT VULCANIZING SYSTEM?

The FDA product code for VINYL POLYSILOXANE 2 COMPONENT VULCANIZING SYSTEM is ELW.

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.

Other records listing Crown Delta Corp. 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.

View all 18 devices →

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.

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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