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FDA 510(k)

DISPERSALLOY-DISPERSED PHASE ALLOY SELF-

K-Number: K802967 · 1980-12-30

ApplicantJohnson & Johnson Professionals, Inc.
Decision Date1980-12-30
Product CodeDZS
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

DISPERSALLOY-DISPERSED PHASE ALLOY SELF- is the device name listed in this FDA 510(k) record. The listed applicant is Johnson & Johnson Professionals, Inc.. It received FDA 510(k) clearance on 1980-12-30 under 510(k) number K802967. The device is classified under product code DZS. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DISPERSALLOY-DISPERSED PHASE ALLOY SELF-?

DISPERSALLOY-DISPERSED PHASE ALLOY SELF- is a medical device that received FDA 510(k) clearance on 1980-12-30. The listed applicant is Johnson & Johnson Professionals, Inc.. The 510(k) number is K802967.

When did DISPERSALLOY-DISPERSED PHASE ALLOY SELF- receive FDA 510(k) clearance?

DISPERSALLOY-DISPERSED PHASE ALLOY SELF- received FDA 510(k) clearance on 1980-12-30, under 510(k) number K802967.

Who is the listed applicant for DISPERSALLOY-DISPERSED PHASE ALLOY SELF-?

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

What is the FDA product code for DISPERSALLOY-DISPERSED PHASE ALLOY SELF-?

The FDA product code for DISPERSALLOY-DISPERSED PHASE ALLOY SELF- is DZS.

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Related Devices (Code: DZS)

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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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