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FDA 510(k)

CSM BETA-LACTAMASE DISC

K-Number: K822518 · 1982-09-21

ApplicantCarr-Scarborough Microbiologicals, Inc.
Decision Date1982-09-21
Product Code
DecisionSubstantially Equivalent

Device Summary

CSM BETA-LACTAMASE DISC 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 1982-09-21 under 510(k) number K822518. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CSM BETA-LACTAMASE DISC?

CSM BETA-LACTAMASE DISC is a medical device that received FDA 510(k) clearance on 1982-09-21. The listed applicant is Carr-Scarborough Microbiologicals, Inc.. The 510(k) number is K822518.

When did CSM BETA-LACTAMASE DISC receive FDA 510(k) clearance?

CSM BETA-LACTAMASE DISC received FDA 510(k) clearance on 1982-09-21, under 510(k) number K822518.

Who is the listed applicant for CSM BETA-LACTAMASE DISC?

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

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Other records listing Carr-Scarborough Microbiologicals, Inc. as applicant

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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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