BANDAGES, SPEC. X-TRA HARD OR PLASTER
K-Number: K770929 · 1977-06-02
Advertisement
Device Summary
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.
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
Advertisement