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FDA 510(k)

PIRD-Y

K-Number: K842262 · 1984-06-28

ApplicantPirdy, Inc.
Decision Date1984-06-28
Product CodeISB
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

PIRD-Y is the device name listed in this FDA 510(k) record. The listed applicant is Pirdy, Inc.. It received FDA 510(k) clearance on 1984-06-28 under 510(k) number K842262. The device is classified under product code ISB. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PIRD-Y?

PIRD-Y is a medical device that received FDA 510(k) clearance on 1984-06-28. The listed applicant is Pirdy, Inc.. The 510(k) number is K842262.

When did PIRD-Y receive FDA 510(k) clearance?

PIRD-Y received FDA 510(k) clearance on 1984-06-28, under 510(k) number K842262.

Who is the listed applicant for PIRD-Y?

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

What is the FDA product code for PIRD-Y?

The FDA product code for PIRD-Y is ISB.

Related Devices (Code: ISB)

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.

K842805IMPULS 3, IT SELECTORRobert Bosch Corp.K790949GALVANIC UNITRami International Corp.K780632MAXICEPTORMed GeneralK780730FIGURETRIMJay-Mar INternational Enterprises, IN

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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