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FDA 510(k)

TELETOM

K-Number: K955750 · 1996-02-08

ApplicantBerchtold Holding GmbH
Decision Date1996-02-08
Product CodeFQO
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

TELETOM is the device name listed in this FDA 510(k) record. The listed applicant is Berchtold Holding GmbH. It received FDA 510(k) clearance on 1996-02-08 under 510(k) number K955750. The device is classified under product code FQO. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TELETOM?

TELETOM is a medical device that received FDA 510(k) clearance on 1996-02-08. The listed applicant is Berchtold Holding GmbH. The 510(k) number is K955750.

When did TELETOM receive FDA 510(k) clearance?

TELETOM received FDA 510(k) clearance on 1996-02-08, under 510(k) number K955750.

Who is the listed applicant for TELETOM?

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

What is the FDA product code for TELETOM?

The FDA product code for TELETOM is FQO.

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Other records listing Berchtold Holding GmbH 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.

K083066CHROMOPHARE E 778 AND E 558K080857CHROMOPHARE E-SERIESK024132CHROMOPHARE X 65K990656CHROMOPHARE D 530 LDR SURGICAL LIGHTK991527CHROMOPHARE D500, D530, D650K974433CHROMOPHARE D 500, CHROMOPHARE D 530

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Related Devices (Code: FQO)

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.

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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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