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FDA 510(k)

LITHOTRITE

K-Number: K760273 · 1976-12-06

ApplicantV. Mueller O.V. Baxter Healthcare Corp.
Decision Date1976-12-06
Product CodeFGK
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

LITHOTRITE is the device name listed in this FDA 510(k) record. The listed applicant is V. Mueller O.V. Baxter Healthcare Corp.. It received FDA 510(k) clearance on 1976-12-06 under 510(k) number K760273. The device is classified under product code FGK. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LITHOTRITE?

LITHOTRITE is a medical device that received FDA 510(k) clearance on 1976-12-06. The listed applicant is V. Mueller O.V. Baxter Healthcare Corp.. The 510(k) number is K760273.

When did LITHOTRITE receive FDA 510(k) clearance?

LITHOTRITE received FDA 510(k) clearance on 1976-12-06, under 510(k) number K760273.

Who is the listed applicant for LITHOTRITE?

The FDA 510(k) record lists V. Mueller O.V. Baxter Healthcare Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LITHOTRITE?

The FDA product code for LITHOTRITE is FGK.

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Other records listing V. Mueller O.V. Baxter Healthcare Corp. 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.

K803292FIELD SUCTION DISSECTORK792383KELMAN DIPSTICKK771197NORTON ENDOTRACHEALK771302PFISTER-SCHWARTZ STONE RETRIEVERK770959BOUGIE, FILIFORM, JACKSONK770280CORD, ELECTROSURGICAL-STERILE & DISPOS.

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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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