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FDA 510(k)

PARKES HUMP GAUGE STRAIGHT 7 (18 CM)

K-Number: K760850 · 1976-11-03

ApplicantV. Mueller O.V. Baxter Healthcare Corp.
Decision Date1976-11-03
Product CodeGDH
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

PARKES HUMP GAUGE STRAIGHT 7 (18 CM) 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 1976-11-03 under 510(k) number K760850. The device is classified under product code GDH. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PARKES HUMP GAUGE STRAIGHT 7 (18 CM)?

PARKES HUMP GAUGE STRAIGHT 7 (18 CM) is a medical device that received FDA 510(k) clearance on 1976-11-03. The listed applicant is V. Mueller O.V. Baxter Healthcare Corp.. The 510(k) number is K760850.

When did PARKES HUMP GAUGE STRAIGHT 7 (18 CM) receive FDA 510(k) clearance?

PARKES HUMP GAUGE STRAIGHT 7 (18 CM) received FDA 510(k) clearance on 1976-11-03, under 510(k) number K760850.

Who is the listed applicant for PARKES HUMP GAUGE STRAIGHT 7 (18 CM)?

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 PARKES HUMP GAUGE STRAIGHT 7 (18 CM)?

The FDA product code for PARKES HUMP GAUGE STRAIGHT 7 (18 CM) is GDH.

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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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Related Devices (Code: GDH)

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.

K903419MODIFIED SURGIPORT DISPOSABLE TROCAR AND SLEEVEUnited States Surgical, A Division of Tyco HealthcK900487MODIFIED AUTO SUTURE SURGIPORT TROCAR & SLEEVEUnited States Surgical, A Division of Tyco HealthcK891901GOUGES, ALEXANDER, BISHOP, LUCASZinnanti Surgical Instruments, Inc.K874879AUTO SUTURE(R) SURGIPORT DISPOS SURG TROCAR/SLEEVEUnited States Surgical, A Division of Tyco HealthcK842822CHERMEL BONE GOUGESCher Mel Corp.

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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