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FDA 510(k)

DIGITAL RADIOGRAPHY SYS DUAL GANTRIES

K-Number: K833237 · 1983-12-08

ApplicantAmerican Science and Engineering, Inc.
Decision Date1983-12-08
Product CodeJAA
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

DIGITAL RADIOGRAPHY SYS DUAL GANTRIES is the device name listed in this FDA 510(k) record. The listed applicant is American Science and Engineering, Inc.. It received FDA 510(k) clearance on 1983-12-08 under 510(k) number K833237. 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 DIGITAL RADIOGRAPHY SYS DUAL GANTRIES?

DIGITAL RADIOGRAPHY SYS DUAL GANTRIES is a medical device that received FDA 510(k) clearance on 1983-12-08. The listed applicant is American Science and Engineering, Inc.. The 510(k) number is K833237.

When did DIGITAL RADIOGRAPHY SYS DUAL GANTRIES receive FDA 510(k) clearance?

DIGITAL RADIOGRAPHY SYS DUAL GANTRIES received FDA 510(k) clearance on 1983-12-08, under 510(k) number K833237.

Who is the listed applicant for DIGITAL RADIOGRAPHY SYS DUAL GANTRIES?

The FDA 510(k) record lists American Science and Engineering, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DIGITAL RADIOGRAPHY SYS DUAL GANTRIES?

The FDA product code for DIGITAL RADIOGRAPHY SYS DUAL GANTRIES is JAA.

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Other records listing American Science and Engineering, Inc. 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.

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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.

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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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