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FDA 510(k)

MODIFIED IDS RAPID NH SYSTEM

K-Number: K881501 · 1988-05-18

ApplicantInnovative Diagnostic Systems, Inc.
Decision Date1988-05-18
Product CodeJSX
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

MODIFIED IDS RAPID NH SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Innovative Diagnostic Systems, Inc.. It received FDA 510(k) clearance on 1988-05-18 under 510(k) number K881501. The device is classified under product code JSX. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODIFIED IDS RAPID NH SYSTEM?

MODIFIED IDS RAPID NH SYSTEM is a medical device that received FDA 510(k) clearance on 1988-05-18. The listed applicant is Innovative Diagnostic Systems, Inc.. The 510(k) number is K881501.

When did MODIFIED IDS RAPID NH SYSTEM receive FDA 510(k) clearance?

MODIFIED IDS RAPID NH SYSTEM received FDA 510(k) clearance on 1988-05-18, under 510(k) number K881501.

Who is the listed applicant for MODIFIED IDS RAPID NH SYSTEM?

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

What is the FDA product code for MODIFIED IDS RAPID NH SYSTEM?

The FDA product code for MODIFIED IDS RAPID NH SYSTEM is JSX.

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 Innovative Diagnostic Systems, 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.

K962966IDS RAPID CB PLUS SYSTEMK943621RAPID YEAST PLUS SYSTEMK900517RAPID NF SYSTEMK882960IDS RAPID ANA SYSTEMK852871IDS RAPID SS/U SYSTEMK852110IDS RAPID E PLUS SYSTEM

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Related Devices (Code: JSX)

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.

K960759GONOPOX TEST KITMedtex Laboratories, Inc.K923566NIZYME TEST KITRemel Co.K913456VISI-NEISSERIAKev Connecticut Diagnostics, Inc.K880511XACT NEISSERIAAustin Biological LaboratoriesK870117NEISSERIA/BRANHAMELLA DIFFERENTIAL TESTPro-Lab, Inc.K853544QUAD FERM +Analytical 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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