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FDA 510(k)

PREAMPLIFIER MODULE, EKG RESPIRATION

K-Number: K790304 · 1979-02-27

ApplicantAbbott Medical Electronics Co.
Decision Date1979-02-27
Product CodeBZQ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

PREAMPLIFIER MODULE, EKG RESPIRATION is the device name listed in this FDA 510(k) record. The listed applicant is Abbott Medical Electronics Co.. It received FDA 510(k) clearance on 1979-02-27 under 510(k) number K790304. The device is classified under product code BZQ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PREAMPLIFIER MODULE, EKG RESPIRATION?

PREAMPLIFIER MODULE, EKG RESPIRATION is a medical device that received FDA 510(k) clearance on 1979-02-27. The listed applicant is Abbott Medical Electronics Co.. The 510(k) number is K790304.

When did PREAMPLIFIER MODULE, EKG RESPIRATION receive FDA 510(k) clearance?

PREAMPLIFIER MODULE, EKG RESPIRATION received FDA 510(k) clearance on 1979-02-27, under 510(k) number K790304.

Who is the listed applicant for PREAMPLIFIER MODULE, EKG RESPIRATION?

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

What is the FDA product code for PREAMPLIFIER MODULE, EKG RESPIRATION?

The FDA product code for PREAMPLIFIER MODULE, EKG RESPIRATION is BZQ.

Related Clinical Trials

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.

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Other records listing Abbott Medical Electronics Co. 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.

K801515ABBY II PATIENT MONITOR OR VITAL SIGNS M

Related Devices (Code: BZQ)

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.

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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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