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)

CALCULATOR PLOTTER (MODEL 9872A)

K-Number: K761055 · 1976-12-09

Decision Date1976-12-09
Product CodeDSF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CALCULATOR PLOTTER (MODEL 9872A) is the device name listed in this FDA 510(k) record. The listed applicant is Hewlett-Packard Co.. It received FDA 510(k) clearance on 1976-12-09 under 510(k) number K761055. The device is classified under product code DSF. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CALCULATOR PLOTTER (MODEL 9872A)?

CALCULATOR PLOTTER (MODEL 9872A) is a medical device that received FDA 510(k) clearance on 1976-12-09. The listed applicant is Hewlett-Packard Co.. The 510(k) number is K761055.

When did CALCULATOR PLOTTER (MODEL 9872A) receive FDA 510(k) clearance?

CALCULATOR PLOTTER (MODEL 9872A) received FDA 510(k) clearance on 1976-12-09, under 510(k) number K761055.

Who is the listed applicant for CALCULATOR PLOTTER (MODEL 9872A)?

The FDA 510(k) record lists Hewlett-Packard Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CALCULATOR PLOTTER (MODEL 9872A)?

The FDA product code for CALCULATOR PLOTTER (MODEL 9872A) is DSF.

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 Hewlett-Packard 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.

View all 230 devices →

Related Devices (Code: DSF)

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.

↑