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FDA 510(k)

PH METER-130 (.001 PH)

K-Number: K760789 · 1976-11-16

Decision Date1976-11-16
Product CodeJQY
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

PH METER-130 (.001 PH) is the device name listed in this FDA 510(k) record. The listed applicant is Corning Medical & Scientific. It received FDA 510(k) clearance on 1976-11-16 under 510(k) number K760789. The device is classified under product code JQY. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PH METER-130 (.001 PH)?

PH METER-130 (.001 PH) is a medical device that received FDA 510(k) clearance on 1976-11-16. The listed applicant is Corning Medical & Scientific. The 510(k) number is K760789.

When did PH METER-130 (.001 PH) receive FDA 510(k) clearance?

PH METER-130 (.001 PH) received FDA 510(k) clearance on 1976-11-16, under 510(k) number K760789.

Who is the listed applicant for PH METER-130 (.001 PH)?

The FDA 510(k) record lists Corning Medical & Scientific as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PH METER-130 (.001 PH)?

The FDA product code for PH METER-130 (.001 PH) is JQY.

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 Corning Medical & Scientific 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 111 devices →

Related Devices (Code: JQY)

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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