Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

METER, IV PH, MODEL ZEROMATIC

K-Number: K770351 · 1977-04-05

Decision Date1977-04-05
Product CodeJQY
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

METER, IV PH, MODEL ZEROMATIC is the device name listed in this FDA 510(k) record. The listed applicant is Beckman Instruments, Inc.. It received FDA 510(k) clearance on 1977-04-05 under 510(k) number K770351. 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 METER, IV PH, MODEL ZEROMATIC?

METER, IV PH, MODEL ZEROMATIC is a medical device that received FDA 510(k) clearance on 1977-04-05. The listed applicant is Beckman Instruments, Inc.. The 510(k) number is K770351.

When did METER, IV PH, MODEL ZEROMATIC receive FDA 510(k) clearance?

METER, IV PH, MODEL ZEROMATIC received FDA 510(k) clearance on 1977-04-05, under 510(k) number K770351.

Who is the listed applicant for METER, IV PH, MODEL ZEROMATIC?

The FDA 510(k) record lists Beckman Instruments, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for METER, IV PH, MODEL ZEROMATIC?

The FDA product code for METER, IV PH, MODEL ZEROMATIC 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 Beckman Instruments, Inc. 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 281 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.

↑