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FDA 510(k)

BANDAGES, SPEC. X-TRA HARD OR PLASTER

K-Number: K770929 · 1977-06-02

Decision Date1977-06-02
Product CodeITG
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

BANDAGES, SPEC. X-TRA HARD OR PLASTER 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 1977-06-02 under 510(k) number K770929. The device is classified under product code ITG. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BANDAGES, SPEC. X-TRA HARD OR PLASTER?

BANDAGES, SPEC. X-TRA HARD OR PLASTER is a medical device that received FDA 510(k) clearance on 1977-06-02. The listed applicant is Johnson & Johnson Professionals, Inc.. The 510(k) number is K770929.

When did BANDAGES, SPEC. X-TRA HARD OR PLASTER receive FDA 510(k) clearance?

BANDAGES, SPEC. X-TRA HARD OR PLASTER received FDA 510(k) clearance on 1977-06-02, under 510(k) number K770929.

Who is the listed applicant for BANDAGES, SPEC. X-TRA HARD OR PLASTER?

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 BANDAGES, SPEC. X-TRA HARD OR PLASTER?

The FDA product code for BANDAGES, SPEC. X-TRA HARD OR PLASTER is ITG.

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 Johnson & Johnson Professionals, 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.

View all 206 devices →

Related Devices (Code: ITG)

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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