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FDA 510(k)

PENTAX F.O.-IT OBSERVER SCOPE

K-Number: K772055 · 1977-11-15

ApplicantPilling Co.
Decision Date1977-11-15
Product Code
DecisionSubstantially Equivalent

Device Summary

PENTAX F.O.-IT OBSERVER SCOPE is the device name listed in this FDA 510(k) record. The listed applicant is Pilling Co.. It received FDA 510(k) clearance on 1977-11-15 under 510(k) number K772055. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PENTAX F.O.-IT OBSERVER SCOPE?

PENTAX F.O.-IT OBSERVER SCOPE is a medical device that received FDA 510(k) clearance on 1977-11-15. The listed applicant is Pilling Co.. The 510(k) number is K772055.

When did PENTAX F.O.-IT OBSERVER SCOPE receive FDA 510(k) clearance?

PENTAX F.O.-IT OBSERVER SCOPE received FDA 510(k) clearance on 1977-11-15, under 510(k) number K772055.

Who is the listed applicant for PENTAX F.O.-IT OBSERVER SCOPE?

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

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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 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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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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