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FDA 510(k)

ARGYLE RAPID GASTRIC LAVAGE KIT

K-Number: K770248 · 1977-03-09

Decision Date1977-03-09
Product CodeKDH
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ARGYLE RAPID GASTRIC LAVAGE KIT is the device name listed in this FDA 510(k) record. The listed applicant is Sherwood Medical Industries. It received FDA 510(k) clearance on 1977-03-09 under 510(k) number K770248. The device is classified under product code KDH. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARGYLE RAPID GASTRIC LAVAGE KIT?

ARGYLE RAPID GASTRIC LAVAGE KIT is a medical device that received FDA 510(k) clearance on 1977-03-09. The listed applicant is Sherwood Medical Industries. The 510(k) number is K770248.

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

ARGYLE RAPID GASTRIC LAVAGE KIT received FDA 510(k) clearance on 1977-03-09, under 510(k) number K770248.

Who is the listed applicant for ARGYLE RAPID GASTRIC LAVAGE KIT?

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

What is the FDA product code for ARGYLE RAPID GASTRIC LAVAGE KIT?

The FDA product code for ARGYLE RAPID GASTRIC LAVAGE KIT is KDH.

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 Sherwood Medical Industries 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 62 devices →

Related Devices (Code: KDH)

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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