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FDA 510(k)

MANAN SELDINGER NEEDLE

K-Number: K851833 · 1985-07-11

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

Device Summary

MANAN SELDINGER 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 K851833. 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 MANAN SELDINGER NEEDLE?

MANAN SELDINGER 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 K851833.

When did MANAN SELDINGER NEEDLE receive FDA 510(k) clearance?

MANAN SELDINGER NEEDLE received FDA 510(k) clearance on 1985-07-11, under 510(k) number K851833.

Who is the listed applicant for MANAN SELDINGER 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 MANAN SELDINGER NEEDLE?

The FDA product code for MANAN SELDINGER 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 NEEDLEK851834MANAN GWI GUIDE WIRE INTRODUCERK852501MYELOGRAM PROCEDURE TRAYK851832NAMAN POTTS COURNAND NEEDLE

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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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