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FDA 510(k)

AP201 DENTAL X-RAY FILM PROCESSOR

K-Number: K900156 · 1990-05-14

ApplicantAllied Photo Products Co., Inc.
Decision Date1990-05-14
Product CodeEGY
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

AP201 DENTAL X-RAY FILM PROCESSOR is the device name listed in this FDA 510(k) record. The listed applicant is Allied Photo Products Co., Inc.. It received FDA 510(k) clearance on 1990-05-14 under 510(k) number K900156. 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 AP201 DENTAL X-RAY FILM PROCESSOR?

AP201 DENTAL X-RAY FILM PROCESSOR is a medical device that received FDA 510(k) clearance on 1990-05-14. The listed applicant is Allied Photo Products Co., Inc.. The 510(k) number is K900156.

When did AP201 DENTAL X-RAY FILM PROCESSOR receive FDA 510(k) clearance?

AP201 DENTAL X-RAY FILM PROCESSOR received FDA 510(k) clearance on 1990-05-14, under 510(k) number K900156.

Who is the listed applicant for AP201 DENTAL X-RAY FILM PROCESSOR?

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

What is the FDA product code for AP201 DENTAL X-RAY FILM PROCESSOR?

The FDA product code for AP201 DENTAL X-RAY FILM PROCESSOR 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.K874118MODEL 410 DENTAL X-RAY FILM PROCESSORSDent-X Co.K811211YOSHIDA AP 100Kaycor Intl., Ltd.

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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