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FDA 510(k)

DENSITOMETER 18, COMPUTING, AUTO.

K-Number: K772325 · 1978-01-12

Decision Date1978-01-12
Product CodeJQT
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

DENSITOMETER 18, COMPUTING, AUTO. is the device name listed in this FDA 510(k) record. The listed applicant is Gelman Instrument Co.. It received FDA 510(k) clearance on 1978-01-12 under 510(k) number K772325. 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 DENSITOMETER 18, COMPUTING, AUTO.?

DENSITOMETER 18, COMPUTING, AUTO. is a medical device that received FDA 510(k) clearance on 1978-01-12. The listed applicant is Gelman Instrument Co.. The 510(k) number is K772325.

When did DENSITOMETER 18, COMPUTING, AUTO. receive FDA 510(k) clearance?

DENSITOMETER 18, COMPUTING, AUTO. received FDA 510(k) clearance on 1978-01-12, under 510(k) number K772325.

Who is the listed applicant for DENSITOMETER 18, COMPUTING, AUTO.?

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

What is the FDA product code for DENSITOMETER 18, COMPUTING, AUTO.?

The FDA product code for DENSITOMETER 18, COMPUTING, AUTO. is JQT.

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 Gelman Instrument Co. 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 11 devices →

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.

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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