FDA 510(k)

TRYPTONE WATER (1%)

K-Number: K864256 · 1987-03-31

Decision Date1987-03-31

Product CodeJSF

Advisory CommitteeMI

DecisionSubstantially Equivalent

Device Summary

TRYPTONE WATER (1%) is the device name listed in this FDA 510(k) record. The listed applicant is Mds Laboratories, Inc.. It received FDA 510(k) clearance on 1987-03-31 under 510(k) number K864256. The device is classified under product code JSF. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRYPTONE WATER (1%)?

TRYPTONE WATER (1%) is a medical device that received FDA 510(k) clearance on 1987-03-31. The listed applicant is Mds Laboratories, Inc.. The 510(k) number is K864256.

When did TRYPTONE WATER (1%) receive FDA 510(k) clearance?

TRYPTONE WATER (1%) received FDA 510(k) clearance on 1987-03-31, under 510(k) number K864256.

Who is the listed applicant for TRYPTONE WATER (1%)?

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

What is the FDA product code for TRYPTONE WATER (1%)?

The FDA product code for TRYPTONE WATER (1%) is JSF.

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Other records listing Mds Laboratories, Inc. as applicant

K864241DNASE AGAR K864242HEKTOEN ENTERIC AGAR K864252THAYER-MARTIN JEMBEC K864247MUELLER HINTON AGAR WITH 5% SHEEP BLOOD K864244GARNERELLA VAGINALIS IDENTIFICATION KIT K864249NORMAL SALINE STERILE

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Related Devices (Code: JSF)

K880946NUTRIENT GELATIN - PRODUCT NUMBER T2860Lakewood Biochemical Co., Inc.K880126LAURYL TRYPTOSE BROTHHardy Media K880119MOELLERS DECARBOXYLASE, ONITHINEHardy Media K880120MOELLERS DECARBOXYLASE, LYSINEHardy Media K880139ONPG TEST REAGENTHardy Media K880113CYSTINE TRYPTIC MEDIUM W/LACTOSEHardy Media

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.