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FDA 510(k)

OCULINUM INJECTION AMPLIFIER

K-Number: K900279 · 1990-02-09

ApplicantOculinum, Inc.
Decision Date1990-02-09
Product CodeHLW
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

OCULINUM INJECTION AMPLIFIER is the device name listed in this FDA 510(k) record. The listed applicant is Oculinum, Inc.. It received FDA 510(k) clearance on 1990-02-09 under 510(k) number K900279. The device is classified under product code HLW. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OCULINUM INJECTION AMPLIFIER?

OCULINUM INJECTION AMPLIFIER is a medical device that received FDA 510(k) clearance on 1990-02-09. The listed applicant is Oculinum, Inc.. The 510(k) number is K900279.

When did OCULINUM INJECTION AMPLIFIER receive FDA 510(k) clearance?

OCULINUM INJECTION AMPLIFIER received FDA 510(k) clearance on 1990-02-09, under 510(k) number K900279.

Who is the listed applicant for OCULINUM INJECTION AMPLIFIER?

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

What is the FDA product code for OCULINUM INJECTION AMPLIFIER?

The FDA product code for OCULINUM INJECTION AMPLIFIER is HLW.

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 Oculinum, Inc. 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.

K900098MONOPOLAR NEEDLE ELECTRODEK854793MONOPOLAR INJECTION NEEDLE ELECTRODE

Related Devices (Code: HLW)

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.

K900098MONOPOLAR NEEDLE ELECTRODEOculinum, Inc.K854793MONOPOLAR INJECTION NEEDLE ELECTRODEOculinum, Inc.

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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