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FDA 510(k)

DTV-4112 FLUOROSCOPIC TELEVISION CAMERA

K-Number: K871127 · 1987-05-01

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

Device Summary

DTV-4112 FLUOROSCOPIC TELEVISION CAMERA 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 K871127. 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-4112 FLUOROSCOPIC TELEVISION CAMERA?

DTV-4112 FLUOROSCOPIC TELEVISION CAMERA 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 K871127.

When did DTV-4112 FLUOROSCOPIC TELEVISION CAMERA receive FDA 510(k) clearance?

DTV-4112 FLUOROSCOPIC TELEVISION CAMERA received FDA 510(k) clearance on 1987-05-01, under 510(k) number K871127.

Who is the listed applicant for DTV-4112 FLUOROSCOPIC TELEVISION CAMERA?

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-4112 FLUOROSCOPIC TELEVISION CAMERA?

The FDA product code for DTV-4112 FLUOROSCOPIC TELEVISION CAMERA is JAA.

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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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