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FDA 510(k)

DAISCOPE & ACCESSORIES

K-Number: K790506 · 1979-04-09

ApplicantSimonsen & Weels Eftf.
Decision Date1979-04-09
Product CodeDRT
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

DAISCOPE & ACCESSORIES is the device name listed in this FDA 510(k) record. The listed applicant is Simonsen & Weels Eftf.. It received FDA 510(k) clearance on 1979-04-09 under 510(k) number K790506. The device is classified under product code DRT. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DAISCOPE & ACCESSORIES?

DAISCOPE & ACCESSORIES is a medical device that received FDA 510(k) clearance on 1979-04-09. The listed applicant is Simonsen & Weels Eftf.. The 510(k) number is K790506.

When did DAISCOPE & ACCESSORIES receive FDA 510(k) clearance?

DAISCOPE & ACCESSORIES received FDA 510(k) clearance on 1979-04-09, under 510(k) number K790506.

Who is the listed applicant for DAISCOPE & ACCESSORIES?

The FDA 510(k) record lists Simonsen & Weels Eftf. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DAISCOPE & ACCESSORIES?

The FDA product code for DAISCOPE & ACCESSORIES is DRT.

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.

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Other records listing Simonsen & Weels Eftf. 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.

K790507800 ECG ELECTRODE

Related Devices (Code: DRT)

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.

K254058DistaSense(TM) (v1)Life Detection TechnologiesK261286The Circadia C300 System (C300)Circadia Health, Inc.K252676The Circadia C300 System (C300)Circadia Health, Inc.K253388Sleepiz One+ (Model 2.5)Sleepiz AGK251364Sleepiz One+ (2.5)Sleepiz AGK234003The Circadia C200 SystemCircadia Technologies, Ltd.

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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