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FDA 510(k)

SILASTIC BRAND PERCUTANEOUS SKIN EXPANDE

K-Number: K801042 · 1980-06-26

ApplicantDow Corning Corp. Healthcare Industries Materials
Decision Date1980-06-26
Product CodeLCJ
DecisionSubstantially Equivalent

Device Summary

SILASTIC BRAND PERCUTANEOUS SKIN EXPANDE is the device name listed in this FDA 510(k) record. The listed applicant is Dow Corning Corp. Healthcare Industries Materials. It received FDA 510(k) clearance on 1980-06-26 under 510(k) number K801042. The device is classified under product code LCJ. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SILASTIC BRAND PERCUTANEOUS SKIN EXPANDE?

SILASTIC BRAND PERCUTANEOUS SKIN EXPANDE is a medical device that received FDA 510(k) clearance on 1980-06-26. The listed applicant is Dow Corning Corp. Healthcare Industries Materials. The 510(k) number is K801042.

When did SILASTIC BRAND PERCUTANEOUS SKIN EXPANDE receive FDA 510(k) clearance?

SILASTIC BRAND PERCUTANEOUS SKIN EXPANDE received FDA 510(k) clearance on 1980-06-26, under 510(k) number K801042.

Who is the listed applicant for SILASTIC BRAND PERCUTANEOUS SKIN EXPANDE?

The FDA 510(k) record lists Dow Corning Corp. Healthcare Industries Materials as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SILASTIC BRAND PERCUTANEOUS SKIN EXPANDE?

The FDA product code for SILASTIC BRAND PERCUTANEOUS SKIN EXPANDE is LCJ.

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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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