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FDA 510(k)

SCANLAN VASCU-STATT

K-Number: K802829 · 1981-01-15

Decision Date1981-01-15
Product CodeFMP
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SCANLAN VASCU-STATT is the device name listed in this FDA 510(k) record. The listed applicant is Scanlan Intl., Inc.. It received FDA 510(k) clearance on 1981-01-15 under 510(k) number K802829. The device is classified under product code FMP. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SCANLAN VASCU-STATT?

SCANLAN VASCU-STATT is a medical device that received FDA 510(k) clearance on 1981-01-15. The listed applicant is Scanlan Intl., Inc.. The 510(k) number is K802829.

When did SCANLAN VASCU-STATT receive FDA 510(k) clearance?

SCANLAN VASCU-STATT received FDA 510(k) clearance on 1981-01-15, under 510(k) number K802829.

Who is the listed applicant for SCANLAN VASCU-STATT?

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

What is the FDA product code for SCANLAN VASCU-STATT?

The FDA product code for SCANLAN VASCU-STATT is FMP.

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 Scanlan Intl., Inc. 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 19 devices →

Related Devices (Code: FMP)

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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