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FDA 510(k)

MODIFIED LABELING FOR TOXI-LAB BROAD SPECTRUM

K-Number: K875181 · 1988-05-27

ApplicantMarion Laboratories, Inc.
Decision Date1988-05-27
Product Code
DecisionSubstantially Equivalent

Device Summary

MODIFIED LABELING FOR TOXI-LAB BROAD SPECTRUM is the device name listed in this FDA 510(k) record. The listed applicant is Marion Laboratories, Inc.. It received FDA 510(k) clearance on 1988-05-27 under 510(k) number K875181. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODIFIED LABELING FOR TOXI-LAB BROAD SPECTRUM?

MODIFIED LABELING FOR TOXI-LAB BROAD SPECTRUM is a medical device that received FDA 510(k) clearance on 1988-05-27. The listed applicant is Marion Laboratories, Inc.. The 510(k) number is K875181.

When did MODIFIED LABELING FOR TOXI-LAB BROAD SPECTRUM receive FDA 510(k) clearance?

MODIFIED LABELING FOR TOXI-LAB BROAD SPECTRUM received FDA 510(k) clearance on 1988-05-27, under 510(k) number K875181.

Who is the listed applicant for MODIFIED LABELING FOR TOXI-LAB BROAD SPECTRUM?

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

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Other records listing Marion 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.

K883391POLYMER ADHESIVE BANDAGEK875182MODIFIED LABELING FOR TOXI-LAB THC SCREENK874554ENVICLUSIVE (TM)K874552ENVISAN PADK874551ENVINET(TM)K874553ENVISAN PASTE

View all 38 devices →

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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