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FDA 510(k)

IDENTICULT-BL

K-Number: K873509 · 1987-10-15

ApplicantScott Laboratories, Inc.
Decision Date1987-10-15
Product CodeJTO
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

IDENTICULT-BL 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 1987-10-15 under 510(k) number K873509. 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 IDENTICULT-BL?

IDENTICULT-BL is a medical device that received FDA 510(k) clearance on 1987-10-15. The listed applicant is Scott Laboratories, Inc.. The 510(k) number is K873509.

When did IDENTICULT-BL receive FDA 510(k) clearance?

IDENTICULT-BL received FDA 510(k) clearance on 1987-10-15, under 510(k) number K873509.

Who is the listed applicant for IDENTICULT-BL?

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 IDENTICULT-BL?

The FDA product code for IDENTICULT-BL 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.

K880694B. CAT CONFIRMK874933MUG-INDOLE DISCK874662MYCO-FLUOR REAGENT A & BK871238ANABAGK863025SERO-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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