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FDA 510(k)

FILM PROCESSOR, AUTOMATIC

K-Number: K770783 · 1977-05-10

ApplicantGeneral Electric Co.
Decision Date1977-05-10
Product CodeEGY
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

FILM PROCESSOR, AUTOMATIC is the device name listed in this FDA 510(k) record. The listed applicant is General Electric Co.. It received FDA 510(k) clearance on 1977-05-10 under 510(k) number K770783. The device is classified under product code EGY. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FILM PROCESSOR, AUTOMATIC?

FILM PROCESSOR, AUTOMATIC is a medical device that received FDA 510(k) clearance on 1977-05-10. The listed applicant is General Electric Co.. The 510(k) number is K770783.

When did FILM PROCESSOR, AUTOMATIC receive FDA 510(k) clearance?

FILM PROCESSOR, AUTOMATIC received FDA 510(k) clearance on 1977-05-10, under 510(k) number K770783.

Who is the listed applicant for FILM PROCESSOR, AUTOMATIC?

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

What is the FDA product code for FILM PROCESSOR, AUTOMATIC?

The FDA product code for FILM PROCESSOR, AUTOMATIC is EGY.

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Other records listing General Electric Co. as applicant

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Related Devices (Code: EGY)

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.

K992896DXSS AUTOMATIC X-RAY FILM PROCESSOR, (MODELS #S: 512, 1530, 812, 830)Dental X-Ray Support Systems, Inc.K955825SMITH S-100 TIME & TEMPERATURE CONTROLSmith Companies Dental ProductsK955643ALARA IMAGING SYSTEMDenoptix, Inc.K945682PROCESSOR, RADIOGRAPHIC-FILM, AUTOMATIC, DENTALGendex Corp.K900156AP201 DENTAL X-RAY FILM PROCESSORAllied Photo Products Co., Inc.K874118MODEL 410 DENTAL X-RAY FILM PROCESSORSDent-X Co.

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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