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FDA 510(k)

SILASTIC BRAND GASTRIC LAVAGE TUBE

K-Number: K760943 · 1976-11-23

ApplicantDow Corning Corp. Healthcare Industries Materials
Decision Date1976-11-23
Product CodeKNY
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

SILASTIC BRAND GASTRIC LAVAGE TUBE 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 1976-11-23 under 510(k) number K760943. The device is classified under product code KNY. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SILASTIC BRAND GASTRIC LAVAGE TUBE?

SILASTIC BRAND GASTRIC LAVAGE TUBE is a medical device that received FDA 510(k) clearance on 1976-11-23. The listed applicant is Dow Corning Corp. Healthcare Industries Materials. The 510(k) number is K760943.

When did SILASTIC BRAND GASTRIC LAVAGE TUBE receive FDA 510(k) clearance?

SILASTIC BRAND GASTRIC LAVAGE TUBE received FDA 510(k) clearance on 1976-11-23, under 510(k) number K760943.

Who is the listed applicant for SILASTIC BRAND GASTRIC LAVAGE TUBE?

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 GASTRIC LAVAGE TUBE?

The FDA product code for SILASTIC BRAND GASTRIC LAVAGE TUBE is KNY.

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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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