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FDA 510(k)

SPOR-TEST-STRIP

K-Number: K801678 · 1980-08-13

ApplicantSterilization Technical Services, Inc.
Decision Date1980-08-13
Product CodeFRC
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SPOR-TEST-STRIP is the device name listed in this FDA 510(k) record. The listed applicant is Sterilization Technical Services, Inc.. It received FDA 510(k) clearance on 1980-08-13 under 510(k) number K801678. The device is classified under product code FRC. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SPOR-TEST-STRIP?

SPOR-TEST-STRIP is a medical device that received FDA 510(k) clearance on 1980-08-13. The listed applicant is Sterilization Technical Services, Inc.. The 510(k) number is K801678.

When did SPOR-TEST-STRIP receive FDA 510(k) clearance?

SPOR-TEST-STRIP received FDA 510(k) clearance on 1980-08-13, under 510(k) number K801678.

Who is the listed applicant for SPOR-TEST-STRIP?

The FDA 510(k) record lists Sterilization Technical Services, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SPOR-TEST-STRIP?

The FDA product code for SPOR-TEST-STRIP is FRC.

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 Sterilization Technical Services, 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.

K812856CHEMICAL INDICATORSK802509G.R.A.M. SLIDE

Related Devices (Code: FRC)

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

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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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