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FDA 510(k)

ESOPHAGEAL BOUGIES

K-Number: K830991 · 1983-06-02

ApplicantMedovations, Inc.
Decision Date1983-06-02
Product CodeKNQ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ESOPHAGEAL BOUGIES is the device name listed in this FDA 510(k) record. The listed applicant is Medovations, Inc.. It received FDA 510(k) clearance on 1983-06-02 under 510(k) number K830991. The device is classified under product code KNQ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ESOPHAGEAL BOUGIES?

ESOPHAGEAL BOUGIES is a medical device that received FDA 510(k) clearance on 1983-06-02. The listed applicant is Medovations, Inc.. The 510(k) number is K830991.

When did ESOPHAGEAL BOUGIES receive FDA 510(k) clearance?

ESOPHAGEAL BOUGIES received FDA 510(k) clearance on 1983-06-02, under 510(k) number K830991.

Who is the listed applicant for ESOPHAGEAL BOUGIES?

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

What is the FDA product code for ESOPHAGEAL BOUGIES?

The FDA product code for ESOPHAGEAL BOUGIES is KNQ.

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Other records listing Medovations, 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.

K002363MEDOVATIONS ESOPHAGEAL DILATORK972119MALONEY BOUGE (1210-XX)/HURST BOUGIE (1212-XX)K924646OVER THE GUIDEWIRE DILATATION SYSTEMK913678TROCAR CATHETERK905478YANKAUER SUCTION DEVICEK874309URETHAL CATHETER

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Related Devices (Code: KNQ)

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.

K122924CRE FIXED WIRE BALLON DILATION CATHETERBoston Scientific CorpK093236ETHICON ENDO-SURGERYOPTICAL DILATOREthicon Endo-Surgery, Inc.K090183HERCULES 3 STAGE WIRE GUIDED DILATION BALLOONCook EndoscopyK082995SMART DILATORSafestitch MedicalK061937COOK ENDOSCOPY ESOPHAGEAL DILATION BALLOONCook EndoscopyK061787MAXFORCE TTS SINGLE-USE BALLOON DILATORBoston Scientific Corp

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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