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FDA 510(k)

JESBERG ESOPHAGOSCOPES W/AUSTINETIC S S

K-Number: K760652 · 1976-12-16

ApplicantPilling Co.
Decision Date1976-12-16
Product CodeEOX
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

JESBERG ESOPHAGOSCOPES W/AUSTINETIC S S is the device name listed in this FDA 510(k) record. The listed applicant is Pilling Co.. It received FDA 510(k) clearance on 1976-12-16 under 510(k) number K760652. The device is classified under product code EOX. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the JESBERG ESOPHAGOSCOPES W/AUSTINETIC S S?

JESBERG ESOPHAGOSCOPES W/AUSTINETIC S S is a medical device that received FDA 510(k) clearance on 1976-12-16. The listed applicant is Pilling Co.. The 510(k) number is K760652.

When did JESBERG ESOPHAGOSCOPES W/AUSTINETIC S S receive FDA 510(k) clearance?

JESBERG ESOPHAGOSCOPES W/AUSTINETIC S S received FDA 510(k) clearance on 1976-12-16, under 510(k) number K760652.

Who is the listed applicant for JESBERG ESOPHAGOSCOPES W/AUSTINETIC S S?

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

What is the FDA product code for JESBERG ESOPHAGOSCOPES W/AUSTINETIC S S?

The FDA product code for JESBERG ESOPHAGOSCOPES W/AUSTINETIC S S is EOX.

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Other records listing Pilling Co. 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.

K934427PILLING LAPAROSCOPIC INSTRUMENTATIONK925370TRIANGULAR JAW MICROLARYNGEAL FORCEPSK925198KAISER NO CANNULA THORACOSCOPY/LAPAROSCOPY INSTRK922971NO-SCALPEL VASCETOMY INSTRUMENTSK914015CLEMENT-PILLING CHOLANGIOGRAPHY CATH GUIDE/CLAMPK911099MEHIGAN-PILLING ANGIOSCOPIC VASCULAR INSTRUM. LINE

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Related Devices (Code: EOX)

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.

K233142EndoSign® Cell collection device (ES-CYT-102)Cyted LimitedK230339EsoCheck Cell Collection DeviceLucid Diagnostics, Inc.K223072PENTAX Medical Video Esophagoscope EE17-J10Pentax of America, Inc.K222366EsoCheck Cell Collection DeviceLucid Diagnostics, Inc.K203450EsophaCap Swallowable Cellular Retrieval Device (changed from Cell-Mata)Capnostics, LLCK210137EsoCheck Cell Collection DeviceLucid Diagnostics, Inc.

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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