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FDA 510(k)

JACKSON ESOPHAGEAL DILATOR

K-Number: K990935 · 1999-05-17

ApplicantPilling Weck Surgical
Decision Date1999-05-17
Product CodeKNQ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

JACKSON ESOPHAGEAL DILATOR is the device name listed in this FDA 510(k) record. The listed applicant is Pilling Weck Surgical. It received FDA 510(k) clearance on 1999-05-17 under 510(k) number K990935. 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 JACKSON ESOPHAGEAL DILATOR?

JACKSON ESOPHAGEAL DILATOR is a medical device that received FDA 510(k) clearance on 1999-05-17. The listed applicant is Pilling Weck Surgical. The 510(k) number is K990935.

When did JACKSON ESOPHAGEAL DILATOR receive FDA 510(k) clearance?

JACKSON ESOPHAGEAL DILATOR received FDA 510(k) clearance on 1999-05-17, under 510(k) number K990935.

Who is the listed applicant for JACKSON ESOPHAGEAL DILATOR?

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

What is the FDA product code for JACKSON ESOPHAGEAL DILATOR?

The FDA product code for JACKSON ESOPHAGEAL DILATOR is KNQ.

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.

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Other records listing Pilling Weck Surgical 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.

K992476PILLING WECK SURGICAL HEART STABILIZER REMOVABLE PADSK992174PILLING WECK SURGICAL AORTIC SPOON-JAW CLAMPK990561OPTICAL FORCEPSK982128SHIKANI-FRENCH SPEAKING VALVE

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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