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FDA 510(k)

GASTRIC LAVAGE KIT-DISPOSABLE

K-Number: K791400 · 1979-08-16

Decision Date1979-08-16
Product CodeGBQ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

GASTRIC LAVAGE KIT-DISPOSABLE is the device name listed in this FDA 510(k) record. The listed applicant is Acumed Instruments Corp.. It received FDA 510(k) clearance on 1979-08-16 under 510(k) number K791400. The device is classified under product code GBQ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GASTRIC LAVAGE KIT-DISPOSABLE?

GASTRIC LAVAGE KIT-DISPOSABLE is a medical device that received FDA 510(k) clearance on 1979-08-16. The listed applicant is Acumed Instruments Corp.. The 510(k) number is K791400.

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

GASTRIC LAVAGE KIT-DISPOSABLE received FDA 510(k) clearance on 1979-08-16, under 510(k) number K791400.

Who is the listed applicant for GASTRIC LAVAGE KIT-DISPOSABLE?

The FDA 510(k) record lists Acumed Instruments Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for GASTRIC LAVAGE KIT-DISPOSABLE?

The FDA product code for GASTRIC LAVAGE KIT-DISPOSABLE is GBQ.

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 Acumed Instruments Corp. 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 8 devices →

Related Devices (Code: GBQ)

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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