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FDA 510(k)

BANDAGES, PLASTER OF PARIS & SPLINTS

K-Number: K770340 · 1977-02-28

ApplicantJohnson & Johnson Professionals, Inc.
Decision Date1977-02-28
Product CodeITG
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

BANDAGES, PLASTER OF PARIS & SPLINTS 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 1977-02-28 under 510(k) number K770340. 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, PLASTER OF PARIS & SPLINTS?

BANDAGES, PLASTER OF PARIS & SPLINTS is a medical device that received FDA 510(k) clearance on 1977-02-28. The listed applicant is Johnson & Johnson Professionals, Inc.. The 510(k) number is K770340.

When did BANDAGES, PLASTER OF PARIS & SPLINTS receive FDA 510(k) clearance?

BANDAGES, PLASTER OF PARIS & SPLINTS received FDA 510(k) clearance on 1977-02-28, under 510(k) number K770340.

Who is the listed applicant for BANDAGES, PLASTER OF PARIS & SPLINTS?

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, PLASTER OF PARIS & SPLINTS?

The FDA product code for BANDAGES, PLASTER OF PARIS & SPLINTS is ITG.

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Related Devices (Code: ITG)

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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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