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FDA 510(k)

ANALYTIC TECH. METAL POINT HEATER #3001

K-Number: K801974 · 1980-11-12

Decision Date1980-11-12
Product CodeELA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ANALYTIC TECH. METAL POINT HEATER #3001 is the device name listed in this FDA 510(k) record. The listed applicant is Analytic Technology. It received FDA 510(k) clearance on 1980-11-12 under 510(k) number K801974. The device is classified under product code ELA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANALYTIC TECH. METAL POINT HEATER #3001?

ANALYTIC TECH. METAL POINT HEATER #3001 is a medical device that received FDA 510(k) clearance on 1980-11-12. The listed applicant is Analytic Technology. The 510(k) number is K801974.

When did ANALYTIC TECH. METAL POINT HEATER #3001 receive FDA 510(k) clearance?

ANALYTIC TECH. METAL POINT HEATER #3001 received FDA 510(k) clearance on 1980-11-12, under 510(k) number K801974.

Who is the listed applicant for ANALYTIC TECH. METAL POINT HEATER #3001?

The FDA 510(k) record lists Analytic Technology as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ANALYTIC TECH. METAL POINT HEATER #3001?

The FDA product code for ANALYTIC TECH. METAL POINT HEATER #3001 is ELA.

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 Analytic Technology 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: ELA)

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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