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FDA 510(k)

MULTI-PORTED FACE PLATE

K-Number: K760654 · 1976-12-06

ApplicantPilling Co.
Decision Date1976-12-06
Product Code
DecisionSubstantially Equivalent

Device Summary

MULTI-PORTED FACE PLATE is the device name listed in this FDA 510(k) record. The listed applicant is Pilling Co.. It received FDA 510(k) clearance on 1976-12-06 under 510(k) number K760654. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MULTI-PORTED FACE PLATE?

MULTI-PORTED FACE PLATE is a medical device that received FDA 510(k) clearance on 1976-12-06. The listed applicant is Pilling Co.. The 510(k) number is K760654.

When did MULTI-PORTED FACE PLATE receive FDA 510(k) clearance?

MULTI-PORTED FACE PLATE received FDA 510(k) clearance on 1976-12-06, under 510(k) number K760654.

Who is the listed applicant for MULTI-PORTED FACE PLATE?

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

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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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