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FDA 510(k)

DTV-411OP

K-Number: K870869 · 1987-05-01

ApplicantAdac Laboratories
Decision Date1987-05-01
Product CodeJAA
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

DTV-411OP is the device name listed in this FDA 510(k) record. The listed applicant is Adac Laboratories. It received FDA 510(k) clearance on 1987-05-01 under 510(k) number K870869. The device is classified under product code JAA. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DTV-411OP?

DTV-411OP is a medical device that received FDA 510(k) clearance on 1987-05-01. The listed applicant is Adac Laboratories. The 510(k) number is K870869.

When did DTV-411OP receive FDA 510(k) clearance?

DTV-411OP received FDA 510(k) clearance on 1987-05-01, under 510(k) number K870869.

Who is the listed applicant for DTV-411OP?

The FDA 510(k) record lists Adac Laboratories as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DTV-411OP?

The FDA product code for DTV-411OP is JAA.

Other records listing Adac 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.

K062298APOLLO GAMMA CAMERA SYSTEMK061029JETSTREAM WORKSPACEK060020AUTOQUANT PLUSK051351PRECEDENCE SPECT/CT IMAGING SYSTEMK042880JETSTREAM WORKSPACEK042903AUTOSPECS

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Related Devices (Code: JAA)

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.

K253103Nexus DRF Digital X-ray Imaging SystemVarex Imaging CorporationK251650Insight Enhanced™ DRF (EN-1002-01)Imaging Engineering, LLCK242488Soteria E-ViewOmega Medical Imaging, LLCK242948Adora DRFi (04550010)Nrt X-Ray A/SK233380TRIDENT Mobile Fluoroscopy SystemDornier Medtech AmericaK233945ProxiDiagnost N90 / Precision CRF (706110, 706400)Philips Medical Systems Dmc GmbH

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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