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FDA 510(k)

PASCO RESISTANT 5 PANEL

K-Number: K853862 · 1986-01-21

Decision Date1986-01-21
Product CodeJWY
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

PASCO RESISTANT 5 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 1986-01-21 under 510(k) number K853862. 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 PASCO RESISTANT 5 PANEL?

PASCO RESISTANT 5 PANEL is a medical device that received FDA 510(k) clearance on 1986-01-21. The listed applicant is Pasco Laboratories, Inc.. The 510(k) number is K853862.

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

PASCO RESISTANT 5 PANEL received FDA 510(k) clearance on 1986-01-21, under 510(k) number K853862.

Who is the listed applicant for PASCO RESISTANT 5 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 PASCO RESISTANT 5 PANEL?

The FDA product code for PASCO RESISTANT 5 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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