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FDA 510(k)

STEAROTHERMOHILUS SPORE STRIPS

K-Number: K800482 · 1980-04-16

ApplicantMdt Corp., Inc.
Decision Date1980-04-16
Product CodeFRC
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

STEAROTHERMOHILUS SPORE STRIPS is the device name listed in this FDA 510(k) record. The listed applicant is Mdt Corp., Inc.. It received FDA 510(k) clearance on 1980-04-16 under 510(k) number K800482. 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 STEAROTHERMOHILUS SPORE STRIPS?

STEAROTHERMOHILUS SPORE STRIPS is a medical device that received FDA 510(k) clearance on 1980-04-16. The listed applicant is Mdt Corp., Inc.. The 510(k) number is K800482.

When did STEAROTHERMOHILUS SPORE STRIPS receive FDA 510(k) clearance?

STEAROTHERMOHILUS SPORE STRIPS received FDA 510(k) clearance on 1980-04-16, under 510(k) number K800482.

Who is the listed applicant for STEAROTHERMOHILUS SPORE STRIPS?

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

What is the FDA product code for STEAROTHERMOHILUS SPORE STRIPS?

The FDA product code for STEAROTHERMOHILUS SPORE STRIPS is FRC.

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Other records listing Mdt Corp., 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.

K960777MDT UNISPORE AND SPOR-TEST BIOLOGICALINDICATORK942485MDT UROLOGY TABLEK942486IMAGE FULL POWER EXAMINATION/MINOR SURGERY TABLEK924380MDT/HARVEY MODEL 7000 & 8000 CHEMICLAVEK926081DENTAL LIGHTK924955MDT/HARVEY MC-8 AND MC-10

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Related Devices (Code: FRC)

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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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