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FDA 510(k)

ACCU PATH STERILE LABEL

K-Number: K904598 · 1990-10-30

ApplicantAccu-Path
Decision Date1990-10-30
Product CodeLDQ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ACCU PATH STERILE LABEL is the device name listed in this FDA 510(k) record. The listed applicant is Accu-Path. It received FDA 510(k) clearance on 1990-10-30 under 510(k) number K904598. The device is classified under product code LDQ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACCU PATH STERILE LABEL?

ACCU PATH STERILE LABEL is a medical device that received FDA 510(k) clearance on 1990-10-30. The listed applicant is Accu-Path. The 510(k) number is K904598.

When did ACCU PATH STERILE LABEL receive FDA 510(k) clearance?

ACCU PATH STERILE LABEL received FDA 510(k) clearance on 1990-10-30, under 510(k) number K904598.

Who is the listed applicant for ACCU PATH STERILE LABEL?

The FDA 510(k) record lists Accu-Path as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ACCU PATH STERILE LABEL?

The FDA product code for ACCU PATH STERILE LABEL is LDQ.

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Related Devices (Code: LDQ)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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