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FDA 510(k)

OLSEN HEGAR NEEDLE HOLDERS

K-Number: K821295 · 1982-06-03

ApplicantConphar, Inc.
Decision Date1982-06-03
Product CodeGDF
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

OLSEN HEGAR NEEDLE HOLDERS is the device name listed in this FDA 510(k) record. The listed applicant is Conphar, Inc.. It received FDA 510(k) clearance on 1982-06-03 under 510(k) number K821295. The device is classified under product code GDF. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OLSEN HEGAR NEEDLE HOLDERS?

OLSEN HEGAR NEEDLE HOLDERS is a medical device that received FDA 510(k) clearance on 1982-06-03. The listed applicant is Conphar, Inc.. The 510(k) number is K821295.

When did OLSEN HEGAR NEEDLE HOLDERS receive FDA 510(k) clearance?

OLSEN HEGAR NEEDLE HOLDERS received FDA 510(k) clearance on 1982-06-03, under 510(k) number K821295.

Who is the listed applicant for OLSEN HEGAR NEEDLE HOLDERS?

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

What is the FDA product code for OLSEN HEGAR NEEDLE HOLDERS?

The FDA product code for OLSEN HEGAR NEEDLE HOLDERS is GDF.

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Other records listing Conphar, 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.

K821825CONPHAR SILICONE FEEDING TUBEK821289MAYO-HEGAR NEEDLE HOLDERK821354CONPHAR MAYO HEGAR NEEDLE HOLDERK821298BACKHAUS CLAMP, 3 1/2K821290LITTAUER SCISSORS 5 1/2K821286IRIS SCISSORS STRAIGHT 4 1/2

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Related Devices (Code: GDF)

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.

K031173NEEDLETECH GUIDEWIRE INTRODUCER NEEDLE, MODELS 40021, 40069, 40053, 40042 & 40013Needle Tech Products, Inc.K950311GLOBAL MEDICAL PRODUCTS BREST LESION LOCALIZATION NEEDLE WITH STIFFENED WIREGlobal Medical Products, Ltd.K950007SURGICAL INSTRUMENT GUIDEUnited States Surgical, A Division of Tyco HealthcK945124BREAST LESION LOCALIZATION NEEDLEPromex, Inc.K944942BREAST LESION LOCALIZATION NEEDLEPromedical , Ltd.K935538BAUER TEMNO COAXIAL NEEDLEBauer Medical, 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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