FDA 510(k)

SILASTIC BRAND Q7-2091 GASTRIC SUMP TUBE

K-Number: K760708 · 1976-11-23

ApplicantDow Corning Corp. Healthcare Industries Materials

Decision Date1976-11-23

Product CodeKNT

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

SILASTIC BRAND Q7-2091 GASTRIC SUMP 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 K760708. The device is classified under product code KNT. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SILASTIC BRAND Q7-2091 GASTRIC SUMP TUBE?

SILASTIC BRAND Q7-2091 GASTRIC SUMP 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 K760708.

When did SILASTIC BRAND Q7-2091 GASTRIC SUMP TUBE receive FDA 510(k) clearance?

SILASTIC BRAND Q7-2091 GASTRIC SUMP TUBE received FDA 510(k) clearance on 1976-11-23, under 510(k) number K760708.

Who is the listed applicant for SILASTIC BRAND Q7-2091 GASTRIC SUMP 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 Q7-2091 GASTRIC SUMP TUBE?

The FDA product code for SILASTIC BRAND Q7-2091 GASTRIC SUMP TUBE is KNT.

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

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Related Devices (Code: KNT)

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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.