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FDA 510(k)

RAKA OCH BOSDA PEANGER

K-Number: K851673 · 1985-05-29

ApplicantGeneral Electric Trading Co.
Decision Date1985-05-29
Product CodeGEN
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

RAKA OCH BOSDA PEANGER is the device name listed in this FDA 510(k) record. The listed applicant is General Electric Trading Co.. It received FDA 510(k) clearance on 1985-05-29 under 510(k) number K851673. The device is classified under product code GEN. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RAKA OCH BOSDA PEANGER?

RAKA OCH BOSDA PEANGER is a medical device that received FDA 510(k) clearance on 1985-05-29. The listed applicant is General Electric Trading Co.. The 510(k) number is K851673.

When did RAKA OCH BOSDA PEANGER receive FDA 510(k) clearance?

RAKA OCH BOSDA PEANGER received FDA 510(k) clearance on 1985-05-29, under 510(k) number K851673.

Who is the listed applicant for RAKA OCH BOSDA PEANGER?

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

What is the FDA product code for RAKA OCH BOSDA PEANGER?

The FDA product code for RAKA OCH BOSDA PEANGER is GEN.

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.

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Other records listing General Electric Trading 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.

K850093PANAMEDIC GAUZE SPONGES

Related Devices (Code: GEN)

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

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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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