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FDA 510(k)

COMPA LAB-R

K-Number: K950765 · 1995-03-13

ApplicantRobert W. Bauer & Assoc., Inc.
Decision Date1995-03-13
Product CodeEBF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

COMPA LAB-R is the device name listed in this FDA 510(k) record. The listed applicant is Robert W. Bauer & Assoc., Inc.. It received FDA 510(k) clearance on 1995-03-13 under 510(k) number K950765. The device is classified under product code EBF. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COMPA LAB-R?

COMPA LAB-R is a medical device that received FDA 510(k) clearance on 1995-03-13. The listed applicant is Robert W. Bauer & Assoc., Inc.. The 510(k) number is K950765.

When did COMPA LAB-R receive FDA 510(k) clearance?

COMPA LAB-R received FDA 510(k) clearance on 1995-03-13, under 510(k) number K950765.

Who is the listed applicant for COMPA LAB-R?

The FDA 510(k) record lists Robert W. Bauer & Assoc., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for COMPA LAB-R?

The FDA product code for COMPA LAB-R is EBF.

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 Robert W. Bauer & Assoc., 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.

K941915ORAL STEEL CARTRIDGE SYRINGEK942219ALGIDENCO AND ALGIPRINT IMPRESSION MATERIALS

Related Devices (Code: EBF)

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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