GASTRIC LAVAGE KIT
K-Number: K780471 · 1978-06-02
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Device Summary
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.
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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