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FDA 510(k)

ABDOMINAL ECG PROCESSOR FOR FETAL MONI.

K-Number: K770295 · 1977-03-09

ApplicantBrattle Instrument Corp.
Decision Date1977-03-09
Product CodeHGI
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

ABDOMINAL ECG PROCESSOR FOR FETAL MONI. is the device name listed in this FDA 510(k) record. The listed applicant is Brattle Instrument Corp.. It received FDA 510(k) clearance on 1977-03-09 under 510(k) number K770295. The device is classified under product code HGI. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ABDOMINAL ECG PROCESSOR FOR FETAL MONI.?

ABDOMINAL ECG PROCESSOR FOR FETAL MONI. is a medical device that received FDA 510(k) clearance on 1977-03-09. The listed applicant is Brattle Instrument Corp.. The 510(k) number is K770295.

When did ABDOMINAL ECG PROCESSOR FOR FETAL MONI. receive FDA 510(k) clearance?

ABDOMINAL ECG PROCESSOR FOR FETAL MONI. received FDA 510(k) clearance on 1977-03-09, under 510(k) number K770295.

Who is the listed applicant for ABDOMINAL ECG PROCESSOR FOR FETAL MONI.?

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

What is the FDA product code for ABDOMINAL ECG PROCESSOR FOR FETAL MONI.?

The FDA product code for ABDOMINAL ECG PROCESSOR FOR FETAL MONI. is HGI.

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Other records listing Brattle Instrument 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.

K810588SYNCHRONIZER #208K802978TRANSCUTANEOUS BLOOD OXYGEN MONITOR #300K781681PHIPIOLOGICAL SYNCHRONIZER PART#205K770692MONITOR, FETAL, NO. L04-1100K770296FETAL MONITOR, PART #101-11009K770297FETAL MONITOR, PART #100-11009

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Related Devices (Code: HGI)

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.

K202915IRIS Thermocoagulator and Digital ColposcopeLiger Medical, LLCK152843Liger Medical HTU-110Liger Medical, LLCK121881DOMAIN SURGICAL SYSTEMDomain Surgical, Inc.K070877ENDOCERVICAL ELECTRODE # 2Modern Medical Equipment Mfg., Ltd.K061651FISCHER CONE BIOPSY EXCISOR, MODELS 900-150, 151, 152, 154, 155, 157 AND 158Apple Medical Corp.K022593THOMAS MEDICAL ELECTRODESThomas Medical, 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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