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FDA 510(k)

GASTRO VAGE SET FOR GASTRIC LAVAGE

K-Number: K822228 · 1982-09-09

ApplicantAckrad Laboratories
Decision Date1982-09-09
Product CodeKNT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

GASTRO VAGE SET FOR GASTRIC LAVAGE is the device name listed in this FDA 510(k) record. The listed applicant is Ackrad Laboratories. It received FDA 510(k) clearance on 1982-09-09 under 510(k) number K822228. 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 GASTRO VAGE SET FOR GASTRIC LAVAGE?

GASTRO VAGE SET FOR GASTRIC LAVAGE is a medical device that received FDA 510(k) clearance on 1982-09-09. The listed applicant is Ackrad Laboratories. The 510(k) number is K822228.

When did GASTRO VAGE SET FOR GASTRIC LAVAGE receive FDA 510(k) clearance?

GASTRO VAGE SET FOR GASTRIC LAVAGE received FDA 510(k) clearance on 1982-09-09, under 510(k) number K822228.

Who is the listed applicant for GASTRO VAGE SET FOR GASTRIC LAVAGE?

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

What is the FDA product code for GASTRO VAGE SET FOR GASTRIC LAVAGE?

The FDA product code for GASTRO VAGE SET FOR GASTRIC LAVAGE is KNT.

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Other records listing Ackrad Laboratories 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.

K021272SIB CATHETER, MODEL 61-7005K020954H/S PROCEDURE TRAY (5F), H/S PROCEDURE TRAY (7F), H/S ELLIPTOSPHERE PROCEDURE TRAY & MULTIPURPOSE PROCEDURE TRAYK020951H/S CATHETER SET (5F), MODEL 61-5005; H/S CATHETER SET (7F), MODEL 61-5007K970492INTRAUTERINE INSEMINATION AND SONOHYSTEROGRAPHY CATHETERK961752H/S CATHETER SET(61-3005, 61-3007, 61-3605, 61-3607)K940176ACKRAD IUI SET FOR INTRAUTERINE INSEMINATION

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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.

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