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FDA 510(k)

PRE-ROLLED TUBULAR STOCKINETTE

K-Number: K831936 · 1983-12-30

ApplicantOrmed Mfg., Inc.
Decision Date1983-12-30
Product Code
DecisionSubstantially Equivalent

Device Summary

PRE-ROLLED TUBULAR STOCKINETTE is the device name listed in this FDA 510(k) record. The listed applicant is Ormed Mfg., Inc.. It received FDA 510(k) clearance on 1983-12-30 under 510(k) number K831936. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PRE-ROLLED TUBULAR STOCKINETTE?

PRE-ROLLED TUBULAR STOCKINETTE is a medical device that received FDA 510(k) clearance on 1983-12-30. The listed applicant is Ormed Mfg., Inc.. The 510(k) number is K831936.

When did PRE-ROLLED TUBULAR STOCKINETTE receive FDA 510(k) clearance?

PRE-ROLLED TUBULAR STOCKINETTE received FDA 510(k) clearance on 1983-12-30, under 510(k) number K831936.

Who is the listed applicant for PRE-ROLLED TUBULAR STOCKINETTE?

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

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Other records listing Ormed Mfg., Inc. as applicant

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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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