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FDA 510(k)

PENTAX LH-150F LIGHT SOURCE

K-Number: K771739 · 1977-09-30

ApplicantPilling Co.
Decision Date1977-09-30
Product CodeFCW
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

PENTAX LH-150F LIGHT SOURCE is the device name listed in this FDA 510(k) record. The listed applicant is Pilling Co.. It received FDA 510(k) clearance on 1977-09-30 under 510(k) number K771739. The device is classified under product code FCW. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PENTAX LH-150F LIGHT SOURCE?

PENTAX LH-150F LIGHT SOURCE is a medical device that received FDA 510(k) clearance on 1977-09-30. The listed applicant is Pilling Co.. The 510(k) number is K771739.

When did PENTAX LH-150F LIGHT SOURCE receive FDA 510(k) clearance?

PENTAX LH-150F LIGHT SOURCE received FDA 510(k) clearance on 1977-09-30, under 510(k) number K771739.

Who is the listed applicant for PENTAX LH-150F LIGHT SOURCE?

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 PENTAX LH-150F LIGHT SOURCE?

The FDA product code for PENTAX LH-150F LIGHT SOURCE is FCW.

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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: FCW)

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.

K123956POWER LED 175KARL STORZ Endoscopy-America, Inc.K123359OVS1 VIDEO SYSTEMOlive Medical Corp.K121724ENDOLIGHT LED 1.1 ENDOLIGHTLED 1.2Richard Wolf Medical Instruments Corp.K093792LED LIGHT SOURCESunoptic Technologies, LLCK091968KARL STORZ LED NOVA 100 COLD LIGHT FOUNTAIN, MODELS 2016020, 20161020CKARL STORZ Endoscopy-America, Inc.K082813STRYKER LED LIGHTSOURCEStryker 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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