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FDA 510(k)

JAZZ PP AGC-O, JAZZ PP

K-Number: K972542 · 1997-07-23

ApplicantTrutone
Decision Date1997-07-23
Product CodeESD
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

JAZZ PP AGC-O, JAZZ PP is the device name listed in this FDA 510(k) record. The listed applicant is Trutone. It received FDA 510(k) clearance on 1997-07-23 under 510(k) number K972542. The device is classified under product code ESD. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the JAZZ PP AGC-O, JAZZ PP?

JAZZ PP AGC-O, JAZZ PP is a medical device that received FDA 510(k) clearance on 1997-07-23. The listed applicant is Trutone. The 510(k) number is K972542.

When did JAZZ PP AGC-O, JAZZ PP receive FDA 510(k) clearance?

JAZZ PP AGC-O, JAZZ PP received FDA 510(k) clearance on 1997-07-23, under 510(k) number K972542.

Who is the listed applicant for JAZZ PP AGC-O, JAZZ PP?

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

What is the FDA product code for JAZZ PP AGC-O, JAZZ PP?

The FDA product code for JAZZ PP AGC-O, JAZZ PP is ESD.

Other records listing Trutone 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.

Related Devices (Code: ESD)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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