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FDA 510(k)

IDS RAPIDS NH SYSTEMS

K-Number: K812048 · 1981-08-18

ApplicantCarr-Scarborough Microbiologicals, Inc.
Decision Date1981-08-18
Product CodeJSX
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

IDS RAPIDS NH SYSTEMS is the device name listed in this FDA 510(k) record. The listed applicant is Carr-Scarborough Microbiologicals, Inc.. It received FDA 510(k) clearance on 1981-08-18 under 510(k) number K812048. 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 IDS RAPIDS NH SYSTEMS?

IDS RAPIDS NH SYSTEMS is a medical device that received FDA 510(k) clearance on 1981-08-18. The listed applicant is Carr-Scarborough Microbiologicals, Inc.. The 510(k) number is K812048.

When did IDS RAPIDS NH SYSTEMS receive FDA 510(k) clearance?

IDS RAPIDS NH SYSTEMS received FDA 510(k) clearance on 1981-08-18, under 510(k) number K812048.

Who is the listed applicant for IDS RAPIDS NH SYSTEMS?

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

What is the FDA product code for IDS RAPIDS NH SYSTEMS?

The FDA product code for IDS RAPIDS NH SYSTEMS is JSX.

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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.

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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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