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FDA 510(k)

VACCON

K-Number: K896733 · 1990-02-01

ApplicantUnoplast A/S
Decision Date1990-02-01
Product CodeKGX
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

VACCON is the device name listed in this FDA 510(k) record. The listed applicant is Unoplast A/S. It received FDA 510(k) clearance on 1990-02-01 under 510(k) number K896733. The device is classified under product code KGX. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VACCON?

VACCON is a medical device that received FDA 510(k) clearance on 1990-02-01. The listed applicant is Unoplast A/S. The 510(k) number is K896733.

When did VACCON receive FDA 510(k) clearance?

VACCON received FDA 510(k) clearance on 1990-02-01, under 510(k) number K896733.

Who is the listed applicant for VACCON?

The FDA 510(k) record lists Unoplast A/S as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VACCON?

The FDA product code for VACCON is KGX.

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 Unoplast A/S 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.

K896734FEEDING TUBEK896729NELATON-, FEMALE - OR TIEMANN CATHETERK896732UNOMETER 500K896730SUCTION CATHETER STRAIGHT/COUDEK896731OXYGEN CATHETERSK802248DISARP ORIGINAL

View all 7 devices →

Related Devices (Code: KGX)

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.

K001240SERAGARD INJECTION PATCHPlatinum Services, Inc.K983368CARE BAND ANTIBACTERIAL BANDAGESAso Corp.K972914SYVEK PATCHMarine Polymer Technologies, Inc.K943314ADHESIVE BANDAGES WITH OTC DRUGJohnson & Johnson Consumer Products, Inc.K952606TARGETT PATCHCutting Edge Technologies, Inc.K954007PARALLELJohnson & Johnson Consumer Products, 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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