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FDA 510(k)

LAP DISCS

K-Number: K905472 · 1991-02-27

ApplicantCarr-Scarborough Microbiologicals, Inc.
Decision Date1991-02-27
Product CodeJTO
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

LAP DISCS 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 1991-02-27 under 510(k) number K905472. The device is classified under product code JTO. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LAP DISCS?

LAP DISCS is a medical device that received FDA 510(k) clearance on 1991-02-27. The listed applicant is Carr-Scarborough Microbiologicals, Inc.. The 510(k) number is K905472.

When did LAP DISCS receive FDA 510(k) clearance?

LAP DISCS received FDA 510(k) clearance on 1991-02-27, under 510(k) number K905472.

Who is the listed applicant for LAP DISCS?

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 LAP DISCS?

The FDA product code for LAP DISCS is JTO.

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Other records listing Carr-Scarborough Microbiologicals, 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.

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Related Devices (Code: JTO)

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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