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FDA 510(k)

PERCUTANEOUS ENDOSCOPIC GASTROSCOPY

K-Number: K833492 · 1983-11-29

ApplicantAmerican Endoscopy, Inc.
Decision Date1983-11-29
Product CodeKNT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

PERCUTANEOUS ENDOSCOPIC GASTROSCOPY is the device name listed in this FDA 510(k) record. The listed applicant is American Endoscopy, Inc.. It received FDA 510(k) clearance on 1983-11-29 under 510(k) number K833492. 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 PERCUTANEOUS ENDOSCOPIC GASTROSCOPY?

PERCUTANEOUS ENDOSCOPIC GASTROSCOPY is a medical device that received FDA 510(k) clearance on 1983-11-29. The listed applicant is American Endoscopy, Inc.. The 510(k) number is K833492.

When did PERCUTANEOUS ENDOSCOPIC GASTROSCOPY receive FDA 510(k) clearance?

PERCUTANEOUS ENDOSCOPIC GASTROSCOPY received FDA 510(k) clearance on 1983-11-29, under 510(k) number K833492.

Who is the listed applicant for PERCUTANEOUS ENDOSCOPIC GASTROSCOPY?

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

What is the FDA product code for PERCUTANEOUS ENDOSCOPIC GASTROSCOPY?

The FDA product code for PERCUTANEOUS ENDOSCOPIC GASTROSCOPY is KNT.

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Other records listing American Endoscopy, 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.

K853274AMERICAN DILATATION SYSTEMK841384PROXIMA 1 PH MONITORK833491ENDO BITE BLOCKK840818BIOPSY FORCEPSK833859TAMPONADE BALLOON CUFFK832458AUTOMATIC ENDOSCOPE

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Related Devices (Code: KNT)

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.

K26189052Fr ViSiGi LUX™; 52Fr ViSiGi 3D®Boehringer Laboratories, LLCK253514Minnesota Four-Lumen Esophagogastric Tamponade Tube - 18 French (0092220); Blakemore Esophageal-Nasogastric Tube - 20 French (0092100); Blakemore Esophageal-Nasogastric Tube - 16 French (0092300)C.R. Bard, Inc.K250389XNY Disposable Gastric Calibration TubeChangzhou Xin Neng Yuan Medical Stapler Co.,LtdK243228Flexi-Seal AIR (with ENFit Connector)ConvatecK242336hygh-tec Drainage IIAmb MedtecK242901ZZIREN™ Orogastric Tube; ZZIREN™ SGT Orogastric Tube - 32 Fr (ZZ-SGT-32); ZZIREN™ SGT Orogastric Tube - 36 Fr (ZZ-SGT-36); ZZIREN™ SGT Orogastric Tube - 40 Fr (ZZ-SGT-40); ZZIREN™ GBT Orogastric Tube - 32 Fr (ZZ-GBT-32); ZZIREN™ GBT Orogastric Tube - 36 Fr (ZZ-GBT-36); ZZIREN™ GBT Orogastric Tube - 40 Fr (ZZ-GBT-40)Tools For Surgery, LLC

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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