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FDA 510(k)

PORGES UNIVERSAL HANDLES

K-Number: K896505 · 1990-01-30

ApplicantPorges Corp.
Decision Date1990-01-30
Product CodeGCP
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

PORGES UNIVERSAL HANDLES is the device name listed in this FDA 510(k) record. The listed applicant is Porges Corp.. It received FDA 510(k) clearance on 1990-01-30 under 510(k) number K896505. The device is classified under product code GCP. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PORGES UNIVERSAL HANDLES?

PORGES UNIVERSAL HANDLES is a medical device that received FDA 510(k) clearance on 1990-01-30. The listed applicant is Porges Corp.. The 510(k) number is K896505.

When did PORGES UNIVERSAL HANDLES receive FDA 510(k) clearance?

PORGES UNIVERSAL HANDLES received FDA 510(k) clearance on 1990-01-30, under 510(k) number K896505.

Who is the listed applicant for PORGES UNIVERSAL HANDLES?

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

What is the FDA product code for PORGES UNIVERSAL HANDLES?

The FDA product code for PORGES UNIVERSAL HANDLES is GCP.

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Other records listing Porges 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.

K900269PORGES DORMIA 3 FR FLAT WIRE BASKET STONE DISLODGEK900031MODIFIED PEDIATRIC SILICONE FOLEY CATHETERSK896503PORGES ERCP CATHETERSK896507PORGES DIATHERMY SNAREK896425PORGES CYTOLOGY BRUSHESK896424PORGES SCLEROTHERAPY NEEDLES

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Related Devices (Code: GCP)

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.

K954614EOS BRAND DISPOSABLE PROCTOSCOPENorth Eos Industries, Inc.K896008MODEL 6500 MERCURY ARC LIGHT SOURCEMedical Dynamics, Inc.K862424STEERABLE CATHETER SYSTEMEndovationsK860103MOD. ENDOPORT SINGLE-USE TROCAR AND SLEEVEEndotherapeuticsK843683MODULAR FIBERSCOPE SYSTEMReichert Scientific InstrumentsK833859TAMPONADE BALLOON CUFFAmerican Endoscopy, 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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