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FDA 510(k)

AP-1 AUTO PROGRAMMER

K-Number: K792590 · 1980-01-04

ApplicantBurdick Corp.
Decision Date1980-01-04
Product CodeIOL
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

AP-1 AUTO PROGRAMMER is the device name listed in this FDA 510(k) record. The listed applicant is Burdick Corp.. It received FDA 510(k) clearance on 1980-01-04 under 510(k) number K792590. The device is classified under product code IOL. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AP-1 AUTO PROGRAMMER?

AP-1 AUTO PROGRAMMER is a medical device that received FDA 510(k) clearance on 1980-01-04. The listed applicant is Burdick Corp.. The 510(k) number is K792590.

When did AP-1 AUTO PROGRAMMER receive FDA 510(k) clearance?

AP-1 AUTO PROGRAMMER received FDA 510(k) clearance on 1980-01-04, under 510(k) number K792590.

Who is the listed applicant for AP-1 AUTO PROGRAMMER?

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

What is the FDA product code for AP-1 AUTO PROGRAMMER?

The FDA product code for AP-1 AUTO PROGRAMMER is IOL.

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Other records listing Burdick Corp. 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.

K942565ALTAIR-DISC RECORDERK941351BURDICK PRO2 OXIMETERK904032ELITE II ELECTROCARDIOGRAPHK903565E560 ELECTROCARDIOGRAPHK900729NEOSERV 824K885085ERGOMED 840/ERGOMED 840L

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Related Devices (Code: IOL)

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.

K950377PARKER MODEL PEParker Treadmill Co., Inc.K950376PARKER MODEL PMParker Treadmill Co., Inc.K925839TRACKMASTERJas Manufacturing Co., Inc.K930261RTM REHABILITATION TREADMILL, MODEL #945-200Biodan Medical Systems, Ltd.K904556MANSFIELD CARDIAC ASSIST MODEL 940(TM) IABBoston Scientific CorpK913518TA620 TREADMILL CONTROLLERSiemens Burdick, Inc.

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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