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FDA 510(k)

REVISED RESISTANT 5 MIC PANEL

K-Number: K864493 · 1987-02-02

Decision Date1987-02-02
Product CodeJWY
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

REVISED RESISTANT 5 MIC PANEL is the device name listed in this FDA 510(k) record. The listed applicant is Pasco Laboratories, Inc.. It received FDA 510(k) clearance on 1987-02-02 under 510(k) number K864493. The device is classified under product code JWY. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the REVISED RESISTANT 5 MIC PANEL?

REVISED RESISTANT 5 MIC PANEL is a medical device that received FDA 510(k) clearance on 1987-02-02. The listed applicant is Pasco Laboratories, Inc.. The 510(k) number is K864493.

When did REVISED RESISTANT 5 MIC PANEL receive FDA 510(k) clearance?

REVISED RESISTANT 5 MIC PANEL received FDA 510(k) clearance on 1987-02-02, under 510(k) number K864493.

Who is the listed applicant for REVISED RESISTANT 5 MIC PANEL?

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

What is the FDA product code for REVISED RESISTANT 5 MIC PANEL?

The FDA product code for REVISED RESISTANT 5 MIC PANEL is JWY.

Related Clinical Trials

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.

Other records listing Pasco 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.

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Related Devices (Code: JWY)

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.

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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