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FDA 510(k)

SITE-MALIS BIPOLAR COAGULATOR MODULE

K-Number: K852075 · 1985-08-20

ApplicantValley Forge Scientific Corp.
Decision Date1985-08-20
Product CodeHQO
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

SITE-MALIS BIPOLAR COAGULATOR MODULE is the device name listed in this FDA 510(k) record. The listed applicant is Valley Forge Scientific Corp.. It received FDA 510(k) clearance on 1985-08-20 under 510(k) number K852075. The device is classified under product code HQO. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SITE-MALIS BIPOLAR COAGULATOR MODULE?

SITE-MALIS BIPOLAR COAGULATOR MODULE is a medical device that received FDA 510(k) clearance on 1985-08-20. The listed applicant is Valley Forge Scientific Corp.. The 510(k) number is K852075.

When did SITE-MALIS BIPOLAR COAGULATOR MODULE receive FDA 510(k) clearance?

SITE-MALIS BIPOLAR COAGULATOR MODULE received FDA 510(k) clearance on 1985-08-20, under 510(k) number K852075.

Who is the listed applicant for SITE-MALIS BIPOLAR COAGULATOR MODULE?

The FDA 510(k) record lists Valley Forge Scientific Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SITE-MALIS BIPOLAR COAGULATOR MODULE?

The FDA product code for SITE-MALIS BIPOLAR COAGULATOR MODULE is HQO.

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Other records listing Valley Forge Scientific Corp. 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.

K050364MALIS 2000 BIPOLAR ELECTROSURGICAL SYSTEMK042604VALLY FORGE SCIENTIFIC MALIS BIPOLAR DISPOSABLE FINGER OPERATED ELECTROSURGICAL INSTRUMENTSK032601STRYKER INTERVENTIONAL PAIN RF GENERATORK033499MALIS IRRIGATION MODULE 1000K982229BI-DENTK973554VALLEY FORGE BIPOLAR BALL TIP ELECTRODE

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Related Devices (Code: HQO)

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.

K070871STARION UNIVERSAL POWER SUPPLYStarion InstrumentsK043155STARION UNIVERSAL POWER SUPPLY (UPS)Starion InstrumentsK002341THERMAL CAUTERY UNIT, MODEL 150Geiger Medical Technologies, Inc.K000893AC POWERED THERMAL CAUTERY UNITStarion InstrumentsK971538MENTOR GEMINI HEMOSTATIC ERASERMentor Ophthalmics, Inc.K962135D.O.R.C. MICRODIATHERMY SYSTEMDutch Ophthalmic USA, 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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