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FDA 510(k)

MAYO-HEGAR NEEDLE HOLDER

K-Number: K821289 · 1982-06-03

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

Device Summary

MAYO-HEGAR NEEDLE HOLDER 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 K821289. 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 MAYO-HEGAR NEEDLE HOLDER?

MAYO-HEGAR NEEDLE HOLDER 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 K821289.

When did MAYO-HEGAR NEEDLE HOLDER receive FDA 510(k) clearance?

MAYO-HEGAR NEEDLE HOLDER received FDA 510(k) clearance on 1982-06-03, under 510(k) number K821289.

Who is the listed applicant for MAYO-HEGAR NEEDLE HOLDER?

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 MAYO-HEGAR NEEDLE HOLDER?

The FDA product code for MAYO-HEGAR NEEDLE HOLDER 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 TUBEK821295OLSEN HEGAR NEEDLE HOLDERSK821354CONPHAR MAYO HEGAR NEEDLE HOLDERK821298BACKHAUS CLAMP, 3 1/2K821290LITTAUER SCISSORS 5 1/2K821286IRIS SCISSORS STRAIGHT 4 1/2

View all 122 devices →

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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