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FDA 510(k)

GASTRIC LAVAGE KIT

K-Number: K780471 · 1978-06-02

Decision Date1978-06-02
Product CodeFAT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

GASTRIC LAVAGE KIT is the device name listed in this FDA 510(k) record. The listed applicant is Gaymar Industries, Inc.. It received FDA 510(k) clearance on 1978-06-02 under 510(k) number K780471. The device is classified under product code FAT. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GASTRIC LAVAGE KIT?

GASTRIC LAVAGE KIT is a medical device that received FDA 510(k) clearance on 1978-06-02. The listed applicant is Gaymar Industries, Inc.. The 510(k) number is K780471.

When did GASTRIC LAVAGE KIT receive FDA 510(k) clearance?

GASTRIC LAVAGE KIT received FDA 510(k) clearance on 1978-06-02, under 510(k) number K780471.

Who is the listed applicant for GASTRIC LAVAGE KIT?

The FDA 510(k) record lists Gaymar Industries, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for GASTRIC LAVAGE KIT?

The FDA product code for GASTRIC LAVAGE KIT is FAT.

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 Gaymar Industries, Inc. 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 27 devices →

Related Devices (Code: FAT)

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

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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