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FDA 510(k)

VACUUM WAND AND UNI-READER

K-Number: K821644 · 1982-06-11

Decision Date1982-06-11
Product CodeILP
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

VACUUM WAND AND UNI-READER is the device name listed in this FDA 510(k) record. The listed applicant is Fred Sammons, Inc.. It received FDA 510(k) clearance on 1982-06-11 under 510(k) number K821644. The device is classified under product code ILP. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VACUUM WAND AND UNI-READER?

VACUUM WAND AND UNI-READER is a medical device that received FDA 510(k) clearance on 1982-06-11. The listed applicant is Fred Sammons, Inc.. The 510(k) number is K821644.

When did VACUUM WAND AND UNI-READER receive FDA 510(k) clearance?

VACUUM WAND AND UNI-READER received FDA 510(k) clearance on 1982-06-11, under 510(k) number K821644.

Who is the listed applicant for VACUUM WAND AND UNI-READER?

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

What is the FDA product code for VACUUM WAND AND UNI-READER?

The FDA product code for VACUUM WAND AND UNI-READER is ILP.

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 Fred Sammons, 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 278 devices →

Related Devices (Code: ILP)

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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