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FDA 510(k)

AIR-SHIELDS VICKERS TELESCAN TELECOM DISPLAY SYST

K-Number: K904691 · 1991-02-19

Decision Date1991-02-19
Product CodeHFM
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

AIR-SHIELDS VICKERS TELESCAN TELECOM DISPLAY SYST is the device name listed in this FDA 510(k) record. The listed applicant is Air-Shields Vickers, Inc.. It received FDA 510(k) clearance on 1991-02-19 under 510(k) number K904691. The device is classified under product code HFM. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AIR-SHIELDS VICKERS TELESCAN TELECOM DISPLAY SYST?

AIR-SHIELDS VICKERS TELESCAN TELECOM DISPLAY SYST is a medical device that received FDA 510(k) clearance on 1991-02-19. The listed applicant is Air-Shields Vickers, Inc.. The 510(k) number is K904691.

When did AIR-SHIELDS VICKERS TELESCAN TELECOM DISPLAY SYST receive FDA 510(k) clearance?

AIR-SHIELDS VICKERS TELESCAN TELECOM DISPLAY SYST received FDA 510(k) clearance on 1991-02-19, under 510(k) number K904691.

Who is the listed applicant for AIR-SHIELDS VICKERS TELESCAN TELECOM DISPLAY SYST?

The FDA 510(k) record lists Air-Shields Vickers, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AIR-SHIELDS VICKERS TELESCAN TELECOM DISPLAY SYST?

The FDA product code for AIR-SHIELDS VICKERS TELESCAN TELECOM DISPLAY SYST is HFM.

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 Air-Shields Vickers, 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 9 devices →

Related Devices (Code: HFM)

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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