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FDA 510(k)

HEADLIGHTS W/ FILTER-OPTICO CABLES

K-Number: K761142 · 1977-01-05

ApplicantPilling Co.
Decision Date1977-01-05
Product CodeFST
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

HEADLIGHTS W/ FILTER-OPTICO CABLES is the device name listed in this FDA 510(k) record. The listed applicant is Pilling Co.. It received FDA 510(k) clearance on 1977-01-05 under 510(k) number K761142. The device is classified under product code FST. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HEADLIGHTS W/ FILTER-OPTICO CABLES?

HEADLIGHTS W/ FILTER-OPTICO CABLES is a medical device that received FDA 510(k) clearance on 1977-01-05. The listed applicant is Pilling Co.. The 510(k) number is K761142.

When did HEADLIGHTS W/ FILTER-OPTICO CABLES receive FDA 510(k) clearance?

HEADLIGHTS W/ FILTER-OPTICO CABLES received FDA 510(k) clearance on 1977-01-05, under 510(k) number K761142.

Who is the listed applicant for HEADLIGHTS W/ FILTER-OPTICO CABLES?

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 HEADLIGHTS W/ FILTER-OPTICO CABLES?

The FDA product code for HEADLIGHTS W/ FILTER-OPTICO CABLES is FST.

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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: FST)

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.

K200874TruView Light Cable, TruView Lateral Retractor Light Cable, Bifurcated Light Cable With Universal EndInnovasis, Inc.K122637LITE DECOMPRESSION SYSTEM- LIGHT CABLE MODEL 48089999Stryker SpineK113697EIGR SURGICAL ILLUMINATION SYSTEMInvuity, Inc.K113330CABLECAPSensormedK102266ISOLED AC-POWERED LED HEADLIGHT SYSTEMIsolux, LLCK101496CABLECAP MODEL: WLF, STZ, ACMSensormed

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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