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)

PANASONIC MODEL HV-5

K-Number: K831150 · 1983-04-28

Decision Date1983-04-28
Product CodeFLL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PANASONIC MODEL HV-5 is the device name listed in this FDA 510(k) record. The listed applicant is Panasonic Co. Div. Matsu Elec. Corp. America. It received FDA 510(k) clearance on 1983-04-28 under 510(k) number K831150. The device is classified under product code FLL. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PANASONIC MODEL HV-5?

PANASONIC MODEL HV-5 is a medical device that received FDA 510(k) clearance on 1983-04-28. The listed applicant is Panasonic Co. Div. Matsu Elec. Corp. America. The 510(k) number is K831150.

When did PANASONIC MODEL HV-5 receive FDA 510(k) clearance?

PANASONIC MODEL HV-5 received FDA 510(k) clearance on 1983-04-28, under 510(k) number K831150.

Who is the listed applicant for PANASONIC MODEL HV-5?

The FDA 510(k) record lists Panasonic Co. Div. Matsu Elec. Corp. America as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PANASONIC MODEL HV-5?

The FDA product code for PANASONIC MODEL HV-5 is FLL.

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 Panasonic Co. Div. Matsu Elec. Corp. America 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 9 devices →

Related Devices (Code: FLL)

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.

↑