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FDA 510(k)

B. CAT CONFIRM

K-Number: K880694 · 1988-06-16

ApplicantScott Laboratories, Inc.
Decision Date1988-06-16
Product CodeJTO
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

B. CAT CONFIRM is the device name listed in this FDA 510(k) record. The listed applicant is Scott Laboratories, Inc.. It received FDA 510(k) clearance on 1988-06-16 under 510(k) number K880694. 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 B. CAT CONFIRM?

B. CAT CONFIRM is a medical device that received FDA 510(k) clearance on 1988-06-16. The listed applicant is Scott Laboratories, Inc.. The 510(k) number is K880694.

When did B. CAT CONFIRM receive FDA 510(k) clearance?

B. CAT CONFIRM received FDA 510(k) clearance on 1988-06-16, under 510(k) number K880694.

Who is the listed applicant for B. CAT CONFIRM?

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

What is the FDA product code for B. CAT CONFIRM?

The FDA product code for B. CAT CONFIRM is JTO.

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Other records listing Scott Laboratories, 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.

K874933MUG-INDOLE DISCK874662MYCO-FLUOR REAGENT A & BK873509IDENTICULT-BLK871238ANABAGK863025SERO-STAT R II STAPHYLOCOCCUS TESTK852869SELECTICULT-CHLAMYDIA

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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.

K050352IN-VITRO DIAGNOSTIC VAGINITIS TEST KITAmeritek Research, LLCK970832PYR SWABRemel, Inc.K970834GRAM SWABRemel, Inc.K970833INDOLE SWABRemel, Inc.K970009LYFO(TM) DIFFERENTIAL DISK-BACITRACINMicrobiologics, Inc.K962966IDS RAPID CB PLUS SYSTEMInnovative Diagnostic Systems, Inc.

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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