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FDA 510(k)

3M ORTHOPEDIC CASTING TAPE

K-Number: K791094 · 1979-07-24

Applicant3M Company
Decision Date1979-07-24
Product CodeITG
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

3M ORTHOPEDIC CASTING TAPE is the device name listed in this FDA 510(k) record. The listed applicant is 3M Company. It received FDA 510(k) clearance on 1979-07-24 under 510(k) number K791094. 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 3M ORTHOPEDIC CASTING TAPE?

3M ORTHOPEDIC CASTING TAPE is a medical device that received FDA 510(k) clearance on 1979-07-24. The listed applicant is 3M Company. The 510(k) number is K791094.

When did 3M ORTHOPEDIC CASTING TAPE receive FDA 510(k) clearance?

3M ORTHOPEDIC CASTING TAPE received FDA 510(k) clearance on 1979-07-24, under 510(k) number K791094.

Who is the listed applicant for 3M ORTHOPEDIC CASTING TAPE?

The FDA 510(k) record lists 3M Company as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for 3M ORTHOPEDIC CASTING TAPE?

The FDA product code for 3M ORTHOPEDIC CASTING TAPE 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 3M Company 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 322 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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