TAPE MEASURE
K-Number: K760521 · 1976-11-12
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Device Summary
Frequently Asked Questions
What is the TAPE MEASURE?
TAPE MEASURE is a medical device that received FDA 510(k) clearance on 1976-11-12. The listed applicant is Mcgaw Laboratories. The 510(k) number is K760521.
When did TAPE MEASURE receive FDA 510(k) clearance?
TAPE MEASURE received FDA 510(k) clearance on 1976-11-12, under 510(k) number K760521.
Who is the listed applicant for TAPE MEASURE?
The FDA 510(k) record lists Mcgaw Laboratories as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TAPE MEASURE?
The FDA product code for TAPE MEASURE is KTZ.
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 Mcgaw Laboratories 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: KTZ)
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.
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