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FDA 510(k)

NAMAN POTTS COURNAND NEEDLE

K-Number: K851832 · 1985-07-11

ApplicantManan Manufacturing Co., Inc.
Decision Date1985-07-11
Product CodeDWS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

NAMAN POTTS COURNAND NEEDLE is the device name listed in this FDA 510(k) record. The listed applicant is Manan Manufacturing Co., Inc.. It received FDA 510(k) clearance on 1985-07-11 under 510(k) number K851832. The device is classified under product code DWS. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NAMAN POTTS COURNAND NEEDLE?

NAMAN POTTS COURNAND NEEDLE is a medical device that received FDA 510(k) clearance on 1985-07-11. The listed applicant is Manan Manufacturing Co., Inc.. The 510(k) number is K851832.

When did NAMAN POTTS COURNAND NEEDLE receive FDA 510(k) clearance?

NAMAN POTTS COURNAND NEEDLE received FDA 510(k) clearance on 1985-07-11, under 510(k) number K851832.

Who is the listed applicant for NAMAN POTTS COURNAND NEEDLE?

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

What is the FDA product code for NAMAN POTTS COURNAND NEEDLE?

The FDA product code for NAMAN POTTS COURNAND NEEDLE is DWS.

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Other records listing Manan Manufacturing Co., Inc. 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.

K873208MANAN TURNER STYLE NEEDLEK864405MANAN CONTRAST MEDIA ADMINISTRATION SETK863848MANAN BREST TUMOR LOCALIZATION NEEDLEK852501MYELOGRAM PROCEDURE TRAYK851833MANAN SELDINGER NEEDLEK851834MANAN GWI GUIDE WIRE INTRODUCER

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Related Devices (Code: DWS)

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.

K022238MYOCARDIAL LEAD IMPLANT TOOL, MODEL 10626Medtronic VascularK964445OCTOPUS TISSUE STABILIZER (28001/28002/28003/28004/28005/28006)Dlp, Inc.K962771BURKE CONGENITAL THORACOSCOPY INSTRUMENTSPilling Weck, Inc.K955689RNS STERILE, DISPOSABLE DIGITAL ANGIOGRAPHIC TRAYContour Fabricators of Florida, Inc.K960139G.E. STERILE ANGIOGRAPHIC TRAYGE Medical SystemsK960144G.E. STERILE CT BIOPSY TRAYGE Medical Systems

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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