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FDA 510(k)

J-TIP NEEDLESS INJECTOR

K-Number: K980082 · 1998-03-04

ApplicantNational Medical Products, Inc.
Decision Date1998-03-04
Product CodeKZE
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

J-TIP NEEDLESS INJECTOR is the device name listed in this FDA 510(k) record. The listed applicant is National Medical Products, Inc.. It received FDA 510(k) clearance on 1998-03-04 under 510(k) number K980082. The device is classified under product code KZE. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the J-TIP NEEDLESS INJECTOR?

J-TIP NEEDLESS INJECTOR is a medical device that received FDA 510(k) clearance on 1998-03-04. The listed applicant is National Medical Products, Inc.. The 510(k) number is K980082.

When did J-TIP NEEDLESS INJECTOR receive FDA 510(k) clearance?

J-TIP NEEDLESS INJECTOR received FDA 510(k) clearance on 1998-03-04, under 510(k) number K980082.

Who is the listed applicant for J-TIP NEEDLESS INJECTOR?

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

What is the FDA product code for J-TIP NEEDLESS INJECTOR?

The FDA product code for J-TIP NEEDLESS INJECTOR is KZE.

Related Clinical Trials

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.

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Other records listing National Medical Products, 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.

K973254J-TIP INJECTOR

Related Devices (Code: KZE)

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.

K121270BIOJECT NEEDLE-FREE INJECTION MANAGEMENT SYSTEMBioject Medical Technologies, Inc.K111517PHARMAJET STRATIS 0.5 ML NEEDLE-FREE INJECTION SYSTEM MODEL 501-01, STRATIS INJECTOR CATALOG 501-10, STRATIS RESET STATIPharmajet, Inc.K110456PHARMAJET 0.1 ML INTRADERMAL NEEDLE-FREE INJECTION SYSTEMPharmajet, Inc.K090959LECTRAJET NEEDLE-FREE INJECTION SYSTEM, MODEL: M3 RAD'Antonio Consultants International, Inc. (Dci)K090003ZETAJETBioject, Inc.K081532PHARMAJET NEEDLE-FREE INJECTION SYSTEMPharmajet, Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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