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FDA 510(k)

LASER CANNISTER FILTER

K-Number: K874615 · 1988-06-23

ApplicantMedical Marketing, Inc.
Decision Date1988-06-23
Product CodeHHR
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

LASER CANNISTER FILTER is the device name listed in this FDA 510(k) record. The listed applicant is Medical Marketing, Inc.. It received FDA 510(k) clearance on 1988-06-23 under 510(k) number K874615. The device is classified under product code HHR. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LASER CANNISTER FILTER?

LASER CANNISTER FILTER is a medical device that received FDA 510(k) clearance on 1988-06-23. The listed applicant is Medical Marketing, Inc.. The 510(k) number is K874615.

When did LASER CANNISTER FILTER receive FDA 510(k) clearance?

LASER CANNISTER FILTER received FDA 510(k) clearance on 1988-06-23, under 510(k) number K874615.

Who is the listed applicant for LASER CANNISTER FILTER?

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

What is the FDA product code for LASER CANNISTER FILTER?

The FDA product code for LASER CANNISTER FILTER is HHR.

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 Medical Marketing, 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.

K874614SUCTION AND LAVAGE PROBEK874611TITANIUM BACKSTOP WITH SUCTIONK874612TITANIUM RODS

Related Devices (Code: HHR)

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.

K881507ENDOCOAGULATOR MODEL 20 LASER & ACCESSORIESHgm Medical Laser Systems, Inc.K871875MODEL 5050 SURGILASER FOR OB-GYN USELasermatic, Inc.K875314GL-35 COLPOSCOPIC LASER SYSTEMLaser Engineering, Inc.K880591LASEGUIDE 600A, 600B, 400A, 400B FOR OB-GYN USELaser Peripherals, LLCK880930MDLS 4000,4900,6000,8000,8900 ND:YAG/1700 C02 LASECopper Lasersonics, Inc.K880991LASER OPTICAL CATHETER SYSTEMMedline Industries, 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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