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FDA 510(k)

MODULAR SCANNING DENSITOMETER SYS.

K-Number: K780318 · 1978-04-12

ApplicantTransidyne General Corp.
Decision Date1978-04-12
Product CodeJQT
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

MODULAR SCANNING DENSITOMETER SYS. is the device name listed in this FDA 510(k) record. The listed applicant is Transidyne General Corp.. It received FDA 510(k) clearance on 1978-04-12 under 510(k) number K780318. The device is classified under product code JQT. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODULAR SCANNING DENSITOMETER SYS.?

MODULAR SCANNING DENSITOMETER SYS. is a medical device that received FDA 510(k) clearance on 1978-04-12. The listed applicant is Transidyne General Corp.. The 510(k) number is K780318.

When did MODULAR SCANNING DENSITOMETER SYS. receive FDA 510(k) clearance?

MODULAR SCANNING DENSITOMETER SYS. received FDA 510(k) clearance on 1978-04-12, under 510(k) number K780318.

Who is the listed applicant for MODULAR SCANNING DENSITOMETER SYS.?

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

What is the FDA product code for MODULAR SCANNING DENSITOMETER SYS.?

The FDA product code for MODULAR SCANNING DENSITOMETER SYS. is JQT.

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Other records listing Transidyne General Corp. 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.

K961217BODILY FLUID DISPOSAL KITK955658LACERATION TRAYK950743ORAL PROCEDURE PACKK950773PROPHYLAXIS PACKK950449SURGICAL BURK950403SURGICAL SAW BLADES

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Related Devices (Code: JQT)

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.

K111356ASIMANAGER - ATArlington Scientific, Inc.K944185ISOSCANIsolab, Inc.K915332MODEL 795 FLUOROMETER/DENSITOMETERCiba Corning Diagnostics Corp.K885254TARGET READERV-Tech, Inc.K860645ELECTROPHORESIS DATA CENTER (EDC)Helena LaboratoriesK862956ICON READERHybritech, Inc.

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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