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FDA 510(k)

AMPLIFIER, PC-700

K-Number: K780116 · 1978-02-24

ApplicantBurdick Corp.
Decision Date1978-02-24
Product CodeDQC
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

AMPLIFIER, PC-700 is the device name listed in this FDA 510(k) record. The listed applicant is Burdick Corp.. It received FDA 510(k) clearance on 1978-02-24 under 510(k) number K780116. The device is classified under product code DQC. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AMPLIFIER, PC-700?

AMPLIFIER, PC-700 is a medical device that received FDA 510(k) clearance on 1978-02-24. The listed applicant is Burdick Corp.. The 510(k) number is K780116.

When did AMPLIFIER, PC-700 receive FDA 510(k) clearance?

AMPLIFIER, PC-700 received FDA 510(k) clearance on 1978-02-24, under 510(k) number K780116.

Who is the listed applicant for AMPLIFIER, PC-700?

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 AMPLIFIER, PC-700?

The FDA product code for AMPLIFIER, PC-700 is DQC.

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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: DQC)

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.

K950537CARDIOPHONICS INCORPORATED DPS 2000 PHONOCARDIOGRAPHCardiophonics, Inc.K952651LIFE SOUND SENSORFlowscan, Inc.K943726ACOUSTIC RECORDERTechnology Applications Assoc., Inc.K924054PHONOCARDIOGRAPHEcho UltrasoundK902185DYNAMIC SPECTRAL PHONOCARDIOGRAPHReeves Scientific, Inc.K900560ACUSON HEARTSOUND/PULSE/RESPIRATION MODULEAcuson Corp.

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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