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FDA 510(k)

AUTO. DEVEL. UNIT FOO DENTAL X-RAY

K-Number: K771433 · 1977-08-19

ApplicantAda Products Co., Inc.
Decision Date1977-08-19
Product CodeEGY
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

AUTO. DEVEL. UNIT FOO DENTAL X-RAY is the device name listed in this FDA 510(k) record. The listed applicant is Ada Products Co., Inc.. It received FDA 510(k) clearance on 1977-08-19 under 510(k) number K771433. 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 AUTO. DEVEL. UNIT FOO DENTAL X-RAY?

AUTO. DEVEL. UNIT FOO DENTAL X-RAY is a medical device that received FDA 510(k) clearance on 1977-08-19. The listed applicant is Ada Products Co., Inc.. The 510(k) number is K771433.

When did AUTO. DEVEL. UNIT FOO DENTAL X-RAY receive FDA 510(k) clearance?

AUTO. DEVEL. UNIT FOO DENTAL X-RAY received FDA 510(k) clearance on 1977-08-19, under 510(k) number K771433.

Who is the listed applicant for AUTO. DEVEL. UNIT FOO DENTAL X-RAY?

The FDA 510(k) record lists Ada Products Co., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AUTO. DEVEL. UNIT FOO DENTAL X-RAY?

The FDA product code for AUTO. DEVEL. UNIT FOO DENTAL X-RAY is EGY.

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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

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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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