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FDA 510(k)

PHIPIOLOGICAL SYNCHRONIZER PART#205

K-Number: K781681 · 1978-10-17

Decision Date1978-10-17
Product CodeIXQ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

PHIPIOLOGICAL SYNCHRONIZER PART#205 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 1978-10-17 under 510(k) number K781681. The device is classified under product code IXQ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PHIPIOLOGICAL SYNCHRONIZER PART#205?

PHIPIOLOGICAL SYNCHRONIZER PART#205 is a medical device that received FDA 510(k) clearance on 1978-10-17. The listed applicant is Brattle Instrument Corp.. The 510(k) number is K781681.

When did PHIPIOLOGICAL SYNCHRONIZER PART#205 receive FDA 510(k) clearance?

PHIPIOLOGICAL SYNCHRONIZER PART#205 received FDA 510(k) clearance on 1978-10-17, under 510(k) number K781681.

Who is the listed applicant for PHIPIOLOGICAL SYNCHRONIZER PART#205?

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 PHIPIOLOGICAL SYNCHRONIZER PART#205?

The FDA product code for PHIPIOLOGICAL SYNCHRONIZER PART#205 is IXQ.

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.

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.

View all 7 devices →

Related Devices (Code: IXQ)

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.

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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