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FDA 510(k)

ASPIRATING ENDO OCULAR PROBE

K-Number: K930123 · 1994-02-16

ApplicantSurgical Technologies, Inc.
Decision Date1994-02-16
Product CodeEQH
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

ASPIRATING ENDO OCULAR PROBE is the device name listed in this FDA 510(k) record. The listed applicant is Surgical Technologies, Inc.. It received FDA 510(k) clearance on 1994-02-16 under 510(k) number K930123. The device is classified under product code EQH. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ASPIRATING ENDO OCULAR PROBE?

ASPIRATING ENDO OCULAR PROBE is a medical device that received FDA 510(k) clearance on 1994-02-16. The listed applicant is Surgical Technologies, Inc.. The 510(k) number is K930123.

When did ASPIRATING ENDO OCULAR PROBE receive FDA 510(k) clearance?

ASPIRATING ENDO OCULAR PROBE received FDA 510(k) clearance on 1994-02-16, under 510(k) number K930123.

Who is the listed applicant for ASPIRATING ENDO OCULAR PROBE?

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

What is the FDA product code for ASPIRATING ENDO OCULAR PROBE?

The FDA product code for ASPIRATING ENDO OCULAR PROBE is EQH.

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Other records listing Surgical Technologies, 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.

K941992CYSTOSCOPEK942029ARTHROSCOPEK946136INFINITECH LIGHTED INFUSION CANNULAK952566OSCILFLATORK951918SURGICAL TECHNOLOGIES, INC. SYRINGEK950683ARTHROGRAM TRAY

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Related Devices (Code: EQH)

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.

K945876WECO ENDOSCOPIC SYSTEM WITH FIBER OPTIC LIGHTWells Johnson Co.K954184JED-LIGHT FIBEROPTIC LIGHT SOURCEJedmed Instrument Co.K951829COLD LIGHT SOURCE LOS 150Laser-Optik-Systeme GmbH & Co. KGK932771BATTERY POWERED, DISPOSABLE ENDOSCOPE LIGHT SOURCEXomed-Treace, Inc.K941661GM OPTI*CAM CAMER WITH DENTAL FIBER OPTIC LIGHTGm Engineering, Inc.K941662GM OPTI*CAM CAMERA WITH ENT FIBER OPTIC LIGHTGm Engineering, 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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