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FDA 510(k)

SILASTIC BRAND G7-2090A

K-Number: K760700 · 1976-11-02

ApplicantDow Corning Corp. Healthcare Industries Materials
Decision Date1976-11-02
Product CodeGCY
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SILASTIC BRAND G7-2090A 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 1976-11-02 under 510(k) number K760700. The device is classified under product code GCY. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SILASTIC BRAND G7-2090A?

SILASTIC BRAND G7-2090A is a medical device that received FDA 510(k) clearance on 1976-11-02. The listed applicant is Dow Corning Corp. Healthcare Industries Materials. The 510(k) number is K760700.

When did SILASTIC BRAND G7-2090A receive FDA 510(k) clearance?

SILASTIC BRAND G7-2090A received FDA 510(k) clearance on 1976-11-02, under 510(k) number K760700.

Who is the listed applicant for SILASTIC BRAND G7-2090A?

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 G7-2090A?

The FDA product code for SILASTIC BRAND G7-2090A is GCY.

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Other records listing Dow Corning Corp. Healthcare Industries Materials as applicant

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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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