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FDA 510(k)

PRE-ROLLED IMPERVIOUS STOCKINETTE

K-Number: K770124 · 1977-01-26

ApplicantNational Patent Development Corp.
Decision Date1977-01-26
Product Code
DecisionSubstantially Equivalent

Device Summary

PRE-ROLLED IMPERVIOUS STOCKINETTE is the device name listed in this FDA 510(k) record. The listed applicant is National Patent Development Corp.. It received FDA 510(k) clearance on 1977-01-26 under 510(k) number K770124. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PRE-ROLLED IMPERVIOUS STOCKINETTE?

PRE-ROLLED IMPERVIOUS STOCKINETTE is a medical device that received FDA 510(k) clearance on 1977-01-26. The listed applicant is National Patent Development Corp.. The 510(k) number is K770124.

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

PRE-ROLLED IMPERVIOUS STOCKINETTE received FDA 510(k) clearance on 1977-01-26, under 510(k) number K770124.

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

The FDA 510(k) record lists National Patent Development Corp. as the applicant. This does not by itself establish the device manufacturer.

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Other records listing National Patent Development Corp. 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.

K843974VARIABLE TEMPERATURE CAUTERY DEVICEK832699HYDRON WOUND DRESSING FAST SEAT KITK822793PIO ROOT CANAL INDICATORK820028ZEON COMPOSITE RESIN LIGHT CURE SYSK820006ZEON COMPOSITE RESIN SYSTEMK811446HYDRON WOUND DRESSING KIT

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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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